ClearanceBrief
510(k) K910799 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

LANDMARK VENOUS ACCESS DEVICE

ApplicantMenlo Care, Inc., Menlo Park CA, US
DecisionSubstantially Equivalent, Mar 21, 1991
ReceivedFeb 25, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910799

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.