Medical Device Manufacturer · IL , Binyamina

Karmelsonix

4 submissions · 4 cleared · Since 2007
4
Total
4
Cleared
0
Denied

Karmelsonix — FDA 510(k) Submissions

Karmelsonix has submitted 4 FDA 510(k) premarket notifications since 2007, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Calculator, Pulmonary Function Interpretor (diagnostic), Recorder, Magnetic Tape, Medical . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
Filters