Medical Device Manufacturer · NL , Oss

Fysicon BV

2 submissions · 2 cleared · Since 2017
2
Total
2
Cleared
0
Denied

Fysicon BV — FDA 510(k) Submissions

Fysicon BV has submitted 2 FDA 510(k) premarket notifications since 2017, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms) . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Cardiovascular 2