Medical Device Manufacturer · US , Dana Point , CA

Ekom S.R.O.

2 submissions · 2 cleared · Since 2006
2
Total
2
Cleared
0
Denied

Ekom S.R.O. — FDA 510(k) Submissions

Ekom S.R.O. has submitted 2 FDA 510(k) premarket notifications since 2006, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Compressor, Air, Portable . Use the specialty filter in the sidebar to narrow results.

2 devices
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All2 Anesthesiology 2