ClearanceBrief
510(k) K883980 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES)

ApplicantMenlo Care, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Dec 5, 1988
ReceivedSep 21, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883980

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.