ClearanceBrief
510(k) K840355 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

DESERET MULTILUMEN SUBCLAVIAN JUGULAR

ApplicantParke-Davis Co., Brookville, Ontario, CA
DecisionSubstantially Equivalent, Mar 19, 1984
ReceivedJan 26, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840355

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.