ClearanceBrief
510(k) K882507 ยท DQX Wire, Guide, Catheter

ACS 0.015 & 0.018 PRESSURE GUIDE WIRE W/MICRO.

ApplicantAdvanced Cardiovascular Systems, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Mar 31, 1989
ReceivedJun 17, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882507

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.