ClearanceBrief
510(k) K823262 ยท DYB Introducer, Catheter

MODEL SP5800 #8 FRENCH INTRO. KIT

ApplicantGould, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jan 18, 1983
ReceivedNov 2, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823262

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.