Sentinel Medical Technologies, LLC

Sentinel Medical Technologies, LLC — FDA 510(k) Submissions

Sentinel Medical Technologies, LLC has submitted 2 FDA 510(k) premarket notifications since 2021, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intra-abdominal Pressure Monitoring Device, Catheter, Retention Type, Balloon . Use the specialty filter in the sidebar to narrow results.