The following data is part of a premarket notification filed by Viz.ai, Inc. with the FDA for Viz Ich.
| Device ID | K210209 |
| 510k Number | K210209 |
| Device Name: | Viz ICH |
| Classification | Radiological Computer-assisted Triage And Notification Software |
| Applicant | Viz.ai, Inc. 350 Rhode Island St, Suite 240 San Francisco, CA 94103 |
| Contact | Gregory Ramina |
| Correspondent | Gregory Ramina Viz.ai, Inc. 350 Rhode Island St, Suite 240 San Francisco, CA 94103 |
| Product Code | QAS |
| CFR Regulation Number | 892.2080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-01-26 |
| Decision Date | 2021-03-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00811852030318 | K210209 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VIZ ICH 88727143 not registered Live/Pending |
Viz.ai, Inc. 2019-12-13 |