Fluke Biomedical

Fluke Biomedical — FDA 510(k) Submissions

Fluke Biomedical has submitted 6 FDA 510(k) premarket notifications since 2008, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm), Tester, Defibrillator . Use the specialty filter in the sidebar to narrow results.