Medical Device Manufacturer · US , Camarillo , CA

The Merlin Corp.

2 submissions · 2 cleared · Since 1994
2
Total
2
Cleared
0
Denied

The Merlin Corp. — FDA 510(k) Submissions

The Merlin Corp. has submitted 2 FDA 510(k) premarket notifications since 1994, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Applicator, Ent Drug, Spirometer, Therapeutic (incentive) . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Ear, Nose, Throat 1 Anesthesiology 1