Medical Device Manufacturer · BR , Itupeva- Sp

Kolplast CI SA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kolplast CI SA Pathology ✕

1 devices

1-1 of 1

Cleared Jan 13, 2017

Kolplast Cervical Sample Collection Kit

Pathology · 442d