Medical Device Manufacturer · US , Roswell , GA

Kimberly-Clark - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2010

Total

Cleared

Denied

Kimberly-Clark has 5 FDA 510(k) cleared medical devices. Based in Roswell, US.

Historical record: 5 cleared submissions from 2010 to 2012. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Kimberly-Clark Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kimberly-Clark

5 devices

1-5 of 5