ClearanceBrief
510(k) K072318 ยท FMF Syringe, Piston

POWRSYRINGE INJECTOR

ApplicantPinyons Medical Technology, Inc., Park City UT, US
DecisionSubstantially Equivalent, Sep 21, 2007
ReceivedAug 20, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072318

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.