ClearanceBrief
510(k) K820834 ยท DYB Introducer, Catheter

PERCOR PERCUTANEOUS INTRODUCER

ApplicantDatascope Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 14, 1982
ReceivedMar 26, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820834

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.