ClearanceBrief
510(k) K062119 ยท DRM Compressor, Cardiac, External

HLR MODEL 601 HEART LUNG RESUSCITATOR AND HEARTSAVER 100

ApplicantMedical Products Mfg., LLC, North Attleboro MA, US
DecisionSubstantially Equivalent, Sep 22, 2006
ReceivedJul 25, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K062119

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.