ClearanceBrief
510(k) K023603 ยท OCY Endoscopic Guidewire, Gastroenterology-Urology

ENDO-GLIDE GUIDEWIRE

ApplicantEndo-Therapeutics, Inc., Safety Harbor FL, US
DecisionSubstantially Equivalent, Feb 19, 2003
ReceivedOct 28, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023603

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.