Kolplast CI SA is one of 60 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.
Kolplast CI SA - FDA 510(k) Cleared Devices
Recent clearances: Kolplast Cervical Sample Collection Kit
1
Total
1
Cleared
0
Denied
Kolplast CI SA has 1 FDA 510(k) cleared medical devices. Based in Itupeva- Sp, BR.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Kolplast CI SA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smith Assoicates as regulatory consultant.
FDA 510(k) Regulatory Record - Kolplast CI SA
1 devices