Medical Device Manufacturer · US , Crofton , MD

Kolplast CI Ltda

1 submissions · 1 cleared · Since 2011
1
Total
1
Cleared
0
Denied

Kolplast CI Ltda — FDA 510(k) Submissions

Kolplast CI Ltda has submitted 1 FDA 510(k) premarket notifications since 2011, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Speculum, Vaginal, Nonmetal . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
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All1 Obstetrics & Gynecology 1