Medical Device Manufacturer · US , Hasbrouck Heights , NJ

Al.Chi.Mi.A

2 submissions · 2 cleared · Since 2003
2
Total
2
Cleared
0
Denied

Al.Chi.Mi.A — FDA 510(k) Submissions

Al.Chi.Mi.A has submitted 2 FDA 510(k) premarket notifications since 2003, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media, Corneal Storage . Use the specialty filter in the sidebar to narrow results.

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