ClearanceBrief
510(k) K081515 ยท FOS Catheter, Umbilical Artery

NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0

ApplicantNeomed, Inc., Swanee GA, US
DecisionSubstantially Equivalent, Jul 21, 2008
ReceivedMay 30, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081515

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.