Propper Mfg. Co., Inc. - FDA 510(k) Cleared Devices
25
Total
25
Cleared
0
Denied
Propper Mfg. Co., Inc. has 25 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 25 cleared submissions from 1977 to 2012. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Propper Mfg. Co., Inc. Filter by specialty or product code using the sidebar.
25 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
Oct 05, 1992
PROPPER SUPER SERACULT(R)
Hematology
174d
Cleared
Mar 20, 1992
PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM.
Anesthesiology
87d
Cleared
Sep 12, 1990
BI-O.K. STEAM TEST-PAK
General Hospital
64d