ClearanceBrief
510(k) K173626 ยท FRC Indicator, Biological Sterilization Process

Celerity 20 Steam Process Challenge Device for Dynamic Air Removal Cycles

ApplicantSTERIS Corporation, Mentor OH, US
DecisionSubstantially Equivalent, Feb 21, 2018
ReceivedNov 24, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173626

DateFirm and productCodeLinked 510(k)
Sep 26, 2022Mckesson Medical-Surgical Inc. Corporate Office
a. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack Steam 3 Inch Length Model Number: LCB053. b. STERIS CORP VERIFY Verify SixCess Sterilization Flash Indicator Strip Steam 2-3/
Open, Classified
FRCNone listed

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