AMICO DH-W35 OPHTHALMOSCOPE SERIES
Mar 2014
272d
Amico Diagnostic Incorporated
1
Total
1
Cleared
0
Denied
Amico Diagnostic Incorporated — FDA 510(k) Submissions
Amico Diagnostic Incorporated has submitted 1 FDA 510(k) premarket notifications since 2014, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Ophthalmoscope, Ac-powered . Use the specialty filter in the sidebar to narrow results.
1 devices