Medical Device Manufacturer · US , Sunnyvale , CA

Renovorx, Inc.

4 submissions · 4 cleared · Since 2014
4
Total
4
Cleared
0
Denied

Renovorx, Inc. — FDA 510(k) Submissions

Renovorx, Inc. has submitted 4 FDA 510(k) premarket notifications since 2014, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular Occluding, Temporary . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 Cardiovascular 4