ClearanceBrief
510(k) K912052 ยท FSM Tray, Surgical, Instrument

HEART CATH TRAY

ApplicantMedical Device Inspection Co., Inc., Great Neck NY, US
DecisionSubstantially Equivalent, Aug 20, 1991
ReceivedMay 9, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912052

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.