ClearanceBrief
510(k) K951159 ยท DQY Catheter, Percutaneous

FASGUIDE

ApplicantTarget Therapeutics, Freemont CA, US
DecisionSubstantially Equivalent, Sep 25, 1995
ReceivedMar 14, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951159

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.