ClearanceBrief
510(k) K100754 ยท FMF Syringe, Piston

GRAFT DELIVERY SYSTEM MODEL SA-6115

ApplicantMicromedics, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Jun 9, 2010
ReceivedMar 17, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100754

No recall in the FDA data names this 510(k).

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