ABLE-X
Jun 2012
97d
Im-Able, Ltd.
1
Total
1
Cleared
0
Denied
Im-Able, Ltd. — FDA 510(k) Submissions
Im-Able, Ltd. has submitted 1 FDA 510(k) premarket notifications since 2012, 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