ClearanceBrief
510(k) K904477 ยท DQX Wire, Guide, Catheter

GUIDEWIRE

ApplicantDatascope Corp., Oakland NJ, US
DecisionSubstantially Equivalent, Dec 6, 1990
ReceivedOct 1, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904477

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.