| Primary Device ID | 00850008977480 |
| NIH Device Record Key | 0e25b1e1-d971-4ab0-aed0-6aa09103f4b3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PowerLook Al Mammo Container- Ferrum v1.0.0 |
| Version Model Number | DSC037-01 |
| Company DUNS | 108870254 |
| Company Name | Icad, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850008977480 [Primary] |
| LMD | System, Digital Image Communications, Radiological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-24 |
| Device Publish Date | 2023-07-14 |
| 00850008977053 - TESTING | 2024-06-18 |
| 00850008977251 - PowerLook Density Assessment V4.0 | 2024-06-18 |
| 00850008977268 - ProFound AI 3.1 | 2024-06-18 |
| 00850008977275 - ProFound AI 3.1 | 2024-06-18 |
| 00850008977282 - TESTING | 2024-06-18 |
| 00850008977299 - PowerLook PRO+ 4GPU Tower Platform, OUS | 2024-06-18 |
| 00850008977305 - PowerLook 10.1.1 | 2024-06-18 |
| 00850008977312 - PowerLook MammoAI Container - Sectra | 2024-06-18 |