Kolplast Cervical Sample Collection Kit
Jan 2017
442d
Kolplast CI SA
1
Total
1
Cleared
0
Denied
Kolplast CI SA — FDA 510(k) Submissions
Kolplast CI SA has submitted 1 FDA 510(k) premarket notifications since 2017, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Spatula, Cervical, Cytological . Use the specialty filter in the sidebar to narrow results.
1 devices