ClearanceBrief
510(k) K242169 ยท DYB Introducer, Catheter

Morph DNA Steerable Introducer Sheath

ApplicantBiocardia, Sunnyvale CA, US
DecisionSubstantially Equivalent, Aug 23, 2024
ReceivedJul 24, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K242169

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.