ClearanceBrief
510(k) K896774 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

STREAMLINE VASCULAR ACCESS DEVICE

ApplicantMenlo Care, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Dec 27, 1989
ReceivedDec 1, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896774

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.