ClearanceBrief
510(k) K821957 ยท KMK Device, Intravascular Catheter Securement

CATH-LOK

ApplicantHpd Medical, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jul 28, 1982
ReceivedJun 30, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821957

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.