Propper Mfg. Co., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
25
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K111453STEAM DOT BLU PROCESS INDICATORApril 5, 2012
K102894CLASSIX CHEMICAL STERILIZATION INDICATORMay 25, 2011
K082620ONCE-A-DAY VERTOS TEST PACKJuly 8, 2009
K031152PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)August 17, 2004
K991618BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATORJanuary 24, 2001
K991276PASS/FAIL CHALLENGE PACKJuly 12, 1999
K973585PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATORNovember 6, 1998
K972747BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)January 9, 1998
K961156ONCE-A-DAY BOWIE AND DICK TEST PACK.April 1, 1997
K921798PROPPER SUPER SERACULT(R)October 5, 1992
K915804PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM.March 20, 1992
K903024BI-O.K. STEAM TEST-PAKSeptember 12, 1990
K895910STEAMLINEAugust 22, 1990
K891784BI-O.K.(TM)-BIOLOGICAL/CHEMICAL INDICATORFebruary 9, 1990
K871672STERILIZATION INDICATOR FOR FLASH STERILIZATIONJune 1, 1987
K851804BIO-CHALLENGE TEST PAKJuly 16, 1985
K834353OK FLASH STERILIZATION INDICATORMarch 19, 1984
K834297PROPPER SERACULTJanuary 27, 1984
K821648GAS CHEX PLASTIC BAGJune 22, 1982
K813204SERACULT OCCULT BLOOF TESTJanuary 28, 1982