STANDEX
May 1989
124d
Alt, Inc.
1
Total
1
Cleared
0
Denied
Alt, Inc. — FDA 510(k) Submissions
Alt, Inc. has submitted 1 FDA 510(k) premarket notifications since 1989, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Exerciser, Non-measuring . Use the specialty filter in the sidebar to narrow results.
1 devices