ClearanceBrief
510(k) K014195 ยท DOX Fluorometer, Lead (Dedicated Instruments)

KAYAK HYDROPHILIC GUIDE WIRES

ApplicantBoston Scientific Corp, Maple Grove MN, US
DecisionSubstantially Equivalent, Mar 19, 2002
ReceivedDec 21, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K014195

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.