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 |