ClearanceBrief
510(k) K882655 ยท DQO Catheter, Intravascular, Diagnostic

PROCEDURE PACKS PRESS. MONITOR/ADMINISTRATION LINE

ApplicantProcedure Packs, Inc., Scottsdale AZ, US
DecisionSubstantially Equivalent, Sep 16, 1988
ReceivedJun 29, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882655

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.