ClearanceBrief
510(k) K823845 ยท FPA Set, Administration, Intravascular

PORT-LOCK

ApplicantNorfolk Medical Products, Inc., Walker MI, US
DecisionSubstantially Equivalent, Mar 1, 1983
ReceivedDec 21, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823845

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.