ClearanceBrief
510(k) K912878 ยท DQX Wire, Guide, Catheter

OPEN ENDED GUIDEWIRE

ApplicantLake Region Mfg., Inc., Chaska MN, US
DecisionSubstantially Equivalent, Sep 11, 1991
ReceivedJul 1, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912878

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.