AMES THERAPY DEVICE
May 2013
169d
Ames Technology, Inc.
1
Total
1
Cleared
0
Denied
Ames Technology, Inc. — FDA 510(k) Submissions
Ames Technology, Inc. has submitted 1 FDA 510(k) premarket notifications since 2013, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Isokinetic Testing And Evaluation . Use the specialty filter in the sidebar to narrow results.
1 devices