ClearanceBrief
510(k) K820736 ยท DQY Catheter, Percutaneous

CENTRAL VENOUS ACCESS CATHETER

ApplicantHemed, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 15, 1982
ReceivedMar 18, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820736

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.