Medical Device Manufacturer · US , Pittsburgh , PA

Nelis

2 submissions · 2 cleared · Since 2015
2
Total
2
Cleared
0
Denied

Nelis — FDA 510(k) Submissions

Nelis has submitted 2 FDA 510(k) premarket notifications since 2015, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Laparoscopic Single Port Access Device . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 General & Plastic Surgery 2