ClearanceBrief
510(k) K811236 ยท DTJ Holder, Heart-Valve, Prosthesis

DISPOSABLE HOLDER FOR HANCOCK AORTIC

ApplicantVascor, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 13, 1981
ReceivedMay 4, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K811236

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.