ClearanceBrief
510(k) K924562 ยท DYB Introducer, Catheter

CATHETER INTRODUCER

ApplicantLuther Medical Products, Inc., Tustin CA, US
DecisionSubstantially Equivalent, Feb 25, 1993
ReceivedSep 9, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924562

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.