ClearanceBrief
510(k) K760392 ยท FMF Syringe, Piston

SYRINGES

ApplicantB. Braun Instruments, Mchenry IL, US
DecisionSubstantially Equivalent, Nov 2, 1976
ReceivedAug 5, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760392

DateFirm and productCodeLinked 510(k)
Aug 26, 2022Mckesson Medical-Surgical Inc. Corporate Office
Perifix LOR Syringe Perifix 8 mL Pouch Luer Lock Tip Without Safety Model Number: 332152
Open, Classified
FMFNone listed

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