ClearanceBrief
510(k) K010497 ยท DQX Wire, Guide, Catheter

SILVERSPEED HYDROPHILIC GUIDEWIRE, MODELS 103-0601-300 AND 103-0602-300

ApplicantMicro Therapeutics, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Mar 22, 2001
ReceivedFeb 21, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K010497

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.