ClearanceBrief
510(k) K915114 ยท DQX Wire, Guide, Catheter

GUIDE WIRE EXTENSION

ApplicantTarget Therapeutics, San Jose CA, US
DecisionSubstantially Equivalent, Feb 11, 1992
ReceivedNov 13, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915114

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.