INVALIFT
Jun 1992
468d
American Invalift Corp.
1
Total
1
Cleared
0
Denied
American Invalift Corp. — FDA 510(k) Submissions
American Invalift Corp. has submitted 1 FDA 510(k) premarket notifications since 1992, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Device, Patient Transfer, Powered . Use the specialty filter in the sidebar to narrow results.
1 devices