ClearanceBrief
510(k) K883613 ยท GDC Table, Operating-Room, Electrical

OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.

ApplicantStierlen-Maquet AG, West Germany, GR
DecisionSubstantially Equivalent, Sep 15, 1988
ReceivedAug 22, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883613

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.