ClearanceBrief
510(k) K940870 ยท FOS Catheter, Umbilical Artery

UMBILI-CATH

ApplicantGesco Intl., Inc., San Antonio TX, US
DecisionSubstantially Equivalent, Aug 2, 1994
ReceivedFeb 25, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940870

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.