Medical Device Manufacturer · US , Walker , MI

Ms. Kate Teaney

1 submissions · 1 cleared · Since 1982
1
Total
1
Cleared
0
Denied

Ms. Kate Teaney — FDA 510(k) Submissions

Ms. Kate Teaney has submitted 1 FDA 510(k) premarket notifications since 1982, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electroglottograph . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Ear, Nose, Throat 1