ClearanceBrief
510(k) K860071 ยท KMK Device, Intravascular Catheter Securement

HOLD-IT FRAMED ADHESIVE FILM

ApplicantVlv Associates, Inc., East Hanover NJ, US
DecisionSubstantially Equivalent, Jan 27, 1986
ReceivedJan 6, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860071

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.