ClearanceBrief
510(k) K841797 ยท DQY Catheter, Percutaneous

MULTIPRO CATHETER

ApplicantShiley, Inc., Walker MI, US
DecisionSubstantially Equivalent, Aug 10, 1984
ReceivedApr 23, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841797

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.