ClearanceBrief
510(k) K972300 ยท JOJ Indicator, Physical/Chemical Sterilization Process

CROSS-CHECKS P

ApplicantSteritec Products Mfg Co, Inc., Castle Rock CO, US
DecisionSubstantially Equivalent, Mar 25, 1998
ReceivedJun 19, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972300

DateFirm and productCodeLinked 510(k)
Apr 29, 2010Steritec Products Mfc. Co., Inc.
Plasma Chemical Sterilization Indicator. Product Numbers Cl 115, PL 173, PL 205.
Terminated
JOJNone listed

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