ClearanceBrief
510(k) K871850 ยท DQX Wire, Guide, Catheter

TELEFLEX STEERABLE GUIDEWIRE

ApplicantTeleflexmedical, Inc., Jeffrey NH, US
DecisionSubstantially Equivalent, Jan 27, 1988
ReceivedMay 12, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871850

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.