ClearanceBrief
510(k) K943147 ยท KMK Device, Intravascular Catheter Securement

STATLOCK CV

ApplicantVenetec, Inc., Newport Beach CA, US
DecisionSubstantially Equivalent, Sep 29, 1994
ReceivedJun 30, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943147

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.