ClearanceBrief
510(k) K993257 ยท DQX Wire, Guide, Catheter

.010 SILVERSPEED HYDROPOPHILIC GUIDEWIRE, .014 SILVERSPED HYDROPHILIC GUIDEWIRE, .016 SILVERSPEED HYDROPHILIC GUIDEWI

ApplicantMicro Therapeutics, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Oct 21, 1999
ReceivedSep 29, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K993257

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.