ClearanceBrief
510(k) K810579 ยท KMK Device, Intravascular Catheter Securement

ADHESIVE I.V. CATHETER DRESSING

ApplicantJohnson & Johnson Professionals, Inc., Raynham MA, US
DecisionSubstantially Equivalent, Mar 26, 1981
ReceivedMar 3, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810579

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.