ClearanceBrief
510(k) K934285 ยท DYB Introducer, Catheter

CATHETER INTRODUCER MODIFICATION

ApplicantDaig Corp., Minnetonka MN, US
DecisionSubstantially Equivalent, Nov 24, 1993
ReceivedAug 27, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934285

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.