RHINOTHERM ULTRA 2
Feb 1990
207d
Twinmed Products, Inc.
1
Total
1
Cleared
0
Denied
Twinmed Products, Inc. — FDA 510(k) Submissions
Twinmed Products, Inc. has submitted 1 FDA 510(k) premarket notifications since 1990, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Humidifier, Non-direct Patient Interface (home-use) . Use the specialty filter in the sidebar to narrow results.
1 devices