Propper Mfg. Co., Inc. - FDA 510(k) Cleared Devices
25
Total
25
Cleared
0
Denied
FDA 510(k) Regulatory Record - Propper Mfg. Co., Inc. General Hospital ✕
17 devices
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
STEAMLINE
General Hospital
316d
Cleared
Feb 09, 1990
BI-O.K.(TM)-BIOLOGICAL/CHEMICAL INDICATOR
General Hospital
322d