Medical Device Manufacturer · US , Deer Field , IL

Padpro, LLC - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

Total

Cleared

Denied

Padpro, LLC has 5 FDA 510(k) cleared medical devices. Based in Deer Field, US.

Historical record: 5 cleared submissions from 2001 to 2002. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Padpro, LLC Filter by specialty or product code using the sidebar.

Padpro, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Padpro, LLC

5 devices

1-5 of 5