ClearanceBrief
510(k) K033321 ยท DQX Wire, Guide, Catheter

SELECTIVA SB GUIDEWIRE

ApplicantNeometrics, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Nov 5, 2003
ReceivedOct 15, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K033321

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.