NANOSEP N10
Apr 1994
162d
Intersep , Ltd.
1
Total
1
Cleared
0
Denied
Intersep , Ltd. — FDA 510(k) Submissions
Intersep , Ltd. has submitted 1 FDA 510(k) premarket notifications since 1994, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Clinical Sample Concentrator . Use the specialty filter in the sidebar to narrow results.
1 devices