ClearanceBrief
510(k) K090036 ยท MED Sterilant, Medical Devices

SYSTEM 1.5 STERILE PROCESSING SYSTEM

ApplicantSTERIS Corporation, Mentor OH, US
DecisionSubstantially Equivalent, Apr 5, 2010
ReceivedJan 6, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090036

DateFirm and productCodeLinked 510(k)
Dec 31, 2013Steris Corporation
SYSTEM 1E Liquid Chemical Sterilant Processing System, Distributed by STERIS Corporation, Mentor, OH The SYSTEM 1E Liquid Chemical Sterilant Processing System is intended for the liquid chemical ster
Terminated
MLRNone listed
Sep 7, 2012Steris Corporation
The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Liquid Sterilant Processing System is intended for the liquid chemical sterilization of manually cleaned immersible and reusable critic
Terminated
MEDNone listed
Aug 28, 2012Steris Corporation
QKC1692E The QKC1692E Quick Connect device connects endoscopes to the sterilization tray for C1220E liquid chemical sterilization processor.
Terminated
MEDNone listed
Jan 25, 2012Steris Corporation Hopkins Facility
STERIS SYSTEM 1E Liquid Chemical Sterilant Processing System. Model P6500, 510 (k) Numbers: K090036 Cleared 4/05/2010; K101409 cleared 8/2/2010; K102462, cleared 9/2/2010; add to file 2/24/2011. The
Terminated
MEDNone listed
Sep 1, 2011Steris Corporation
SYSTEM 1E Liquid Chemical Sterilant Processing System, Model # P6500, S/N: 400001 through 405005; Mfr. By: STERIS Corporation, Mentor, OH 44060. Product Usage: The SYSTEM 1E Liquid Chemical Sterilan
Terminated
MLRNone listed
Apr 12, 2011Steris Corporation Hopkins Facility
STERIS SYSTEM 1E Liquid Chemical Sterilant Processing System The SYSTEM 1 E Liquid Chemical Sterilant Processing System is intended for the liquid chemical sterilization of manually cleaned impressib
Terminated
MEDNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.