ClearanceBrief
510(k) K011287 ยท DQX Wire, Guide, Catheter

RADIUS COUGAR WIRE

ApplicantRadius Medical Technologies, Inc., Hopkonton MA, US
DecisionSubstantially Equivalent, May 25, 2001
ReceivedApr 27, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K011287

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.