ClearanceBrief
510(k) K073596 ยท FOS Catheter, Umbilical Artery

NEOMED SINGLE LUMEN UMBILICAL CATHETER

ApplicantNeomed, Inc., Swanee GA, US
DecisionSubstantially Equivalent, Feb 22, 2008
ReceivedDec 21, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073596

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.