Medical Device Manufacturer · US , Mchenry , IL

Propper Mfg. Co., Inc. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1977

25

Total

25

Cleared

0

Denied

FDA 510(k) Regulatory Record - Propper Mfg. Co., Inc. General Hospital ✕

17 devices

1-12 of 17

Cleared Apr 05, 2012

STEAM DOT BLU PROCESS INDICATOR

General Hospital · 316d

Cleared May 25, 2011

CLASSIX CHEMICAL STERILIZATION INDICATOR

General Hospital · 237d

Cleared Jul 08, 2009

ONCE-A-DAY VERTOS TEST PACK

General Hospital · 302d

Cleared Aug 17, 2004

PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)

General Hospital · 494d

Cleared Jan 24, 2001

BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATOR

General Hospital · 624d

Cleared Jul 12, 1999

PASS/FAIL CHALLENGE PACK

General Hospital · 89d

Cleared Nov 06, 1998

PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR

General Hospital · 410d

Cleared Jan 09, 1998

BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)

General Hospital · 170d

Cleared Apr 01, 1997

ONCE-A-DAY BOWIE AND DICK TEST PACK.

General Hospital · 375d

Cleared Sep 12, 1990

BI-O.K. STEAM TEST-PAK

General Hospital · 64d

Cleared Aug 22, 1990

General Hospital · 316d

Cleared Feb 09, 1990

BI-O.K.(TM)-BIOLOGICAL/CHEMICAL INDICATOR

General Hospital · 322d