ClearanceBrief
510(k) K770403 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

CATHETER-THRU-NEEDLE DEVICE

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, Mar 16, 1977
ReceivedMar 3, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770403

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.