ClearanceBrief
510(k) K002786 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

BIOSENSORS CENTRAL VENOUS CATHETER KITS

ApplicantSunscope Intl., Inc., Newport Beach CA, US
DecisionSubstantially Equivalent, Nov 17, 2000
ReceivedSep 7, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002786

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.