A1 ACOUSTIC RHINOMETER
Sep 1998
481d
G.M. Instruments , Ltd.
1
Total
1
Cleared
0
Denied
G.M. Instruments , Ltd. — FDA 510(k) Submissions
G.M. Instruments , Ltd. has submitted 1 FDA 510(k) premarket notifications since 1998, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Rhinoanemometer (measurement Of Nasal Decongestion) . Use the specialty filter in the sidebar to narrow results.
1 devices