ClearanceBrief
510(k) K910280 ยท DQX Wire, Guide, Catheter

ULTRA-SELECT PTCA GUIDEWIRE

ApplicantMicrovena Corp., Findley MN, US
DecisionSubstantially Equivalent, Apr 19, 1991
ReceivedJan 23, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910280

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.