ClearanceBrief
510(k) K850884 ยท FOS Catheter, Umbilical Artery

ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER

ApplicantSherwood Medical Co., St. Louis MO, US
DecisionSubstantially Equivalent, Oct 17, 1985
ReceivedMar 4, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850884

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.