| Primary Device ID | 00850921007172 |
| NIH Device Record Key | 970e37a4-6db9-4ce5-90d3-63138d85189a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SeeMore Software |
| Version Model Number | 4.4.x |
| Company DUNS | 079884004 |
| Company Name | INTERSON CORP |
| 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 | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
| Phone | 925-462-4948 |
| orders@interson.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850921007172 [Primary] |
| IYO | System, Imaging, Pulsed Echo, Ultrasonic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-05-23 |
| Device Publish Date | 2017-06-13 |
| 00850921007172 | SeeMore Software 4.4.x |
| 00850921007165 | SeeMore Software 4.2.1 Urology |
| 00850921007158 | SeeMore Software 4.2.1 Generic |
| 00850921007141 | SeeMore Software 4.2.1 OB GYN |
| 00850921007110 | SeeMore Software 2.0.03 OB GYN |
| 00850921007103 | SeeMore Software 2.0.03 Generic |
| 00850921007066 | SeeMore Software 2.0.03 Urology |