INSIDE VIEW
Jul 2000
85d
Monadnock Optics, Inc.
1
Total
1
Cleared
0
Denied
Monadnock Optics, Inc. — FDA 510(k) Submissions
Monadnock Optics, Inc. has submitted 1 FDA 510(k) premarket notifications since 2000, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Endoscope, Rigid . Use the specialty filter in the sidebar to narrow results.
1 devices