Medical Device Manufacturer · US , Deer Field , IL

Padpro, LLC - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

Recent clearances: PADPRO, MODEL 2502, PADPRO MODEL #2516, PADPRO, MODEL 2603

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Padpro, LLC Cardiovascular ✕

5 devices

1-5 of 5

Cleared May 28, 2002

PADPRO, MODEL 2502

Cardiovascular · 83d

Cleared May 08, 2002

PADPRO MODEL #2516

Cardiovascular · 106d

Cleared Feb 27, 2002

PADPRO, MODEL 2603

Cardiovascular · 30d

Cleared Jan 18, 2002

PADPRO MODEL 2001, 2001-S, 2001-C, 2001-EPS

Cardiovascular · 28d

Cleared Sep 04, 2001

PADPRO SYSTEM DEFIBRILLATOR ELECTRODE ADAPTERS

Cardiovascular · 291d