ClearanceBrief
510(k) K954300 ยท FOS Catheter, Umbilical Artery

ARGYLE NEO-SERT HYDROPHILIC POLYURETHANE UMBILICAL VESSEL CATHETER INSERTION TRAY

ApplicantSherwood Medical Co., St. Louis MO, US
DecisionSubstantially Equivalent, Dec 13, 1995
ReceivedSep 14, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954300

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.