QuickClear P3223ASP
GUDID 00813132029869
QuickClear Aspiration Pump
Philips Image Guided Therapy Corporation
Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use Thrombectomy electric suction pump, single-use| Primary Device ID | 00813132029869 |
| NIH Device Record Key | 7e36225f-a06e-4120-a9e4-d8d90dcb9570 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | QuickClear |
| Version Model Number | P3223ASP |
| Catalog Number | P3223ASP |
| Company DUNS | 118354223 |
| Company Name | Philips Image Guided Therapy Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813132029869 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K193197
FDA Product Code
| QEZ | Aspiration Thrombectomy Catheter |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-19 |
| Device Publish Date | 2023-06-09 |
Devices Manufactured by Philips Image Guided Therapy Corporation
| 20813132029412 - Quick-Cross Extreme | 2023-10-12 Quick-Cross Extreme Support Catheter |
| 20813132029429 - Quick-Cross Extreme | 2023-10-12 Quick-Cross Extreme Support Catheter |
| 20813132029436 - Quick-Cross Extreme | 2023-10-12 Quick-Cross Extreme Support Catheter |
| 20813132029443 - Quick-Cross Extreme | 2023-10-12 Quick-Cross Extreme Support Catheter |
| 20813132029450 - Quick-Cross Extreme | 2023-10-12 Quick-Cross Extreme Support Catheter |
| 00813132029463 - Quick-Cross Extreme | 2023-10-12 Quick-Cross Extreme Support Catheter |
| 20813132029474 - Quick-Cross Extreme | 2023-10-12 Quick-Cross Extreme Support Catheter |
| 20813132029481 - Quick-Cross Extreme | 2023-10-12 Quick-Cross Extreme Support Catheter |
Trademark Results [QuickClear]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 QUICKCLEAR 86113264 4696925 Live/Registered |
Ford Motor Company 2013-11-08 |
 QUICKCLEAR 78903906 3396350 Dead/Cancelled |
RT Lawrence Corporation 2006-06-08 |
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