Medical Device Manufacturer · US , Mchenry , IL

Procedure Products, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1981

16

Total

16

Cleared

0

Denied

FDA 510(k) Regulatory Record - Procedure Products, Inc. Cardiovascular ✕

6 devices

1-6 of 6

Cleared Dec 10, 1992

Cardiovascular · 196d

Cleared Nov 27, 1991

Cardiovascular · 75d

Cleared Jan 29, 1988

ANGIO WASTE FLUIDS DUMP BAG

Cardiovascular · 116d

Cleared Jan 13, 1986

CUSTOM CORONARY MANIFOLD KITS

Cardiovascular · 126d

Cleared Mar 12, 1984

MATERIAL ADDITION LEXAN & K-RESIN

Cardiovascular · 159d

Cleared Apr 11, 1981

SINGLE USE SELDINGER/COURNAND PERC. NDL

Cardiovascular · 12d