ClearanceBrief
510(k) K896421 ยท KMK Device, Intravascular Catheter Securement

TRANSPARENT FILM I.V. SITE/WOUND DRESSING

ApplicantCatalina Biomedical Corp., Duarte CA, US
DecisionSubstantially Equivalent, Jan 31, 1990
ReceivedNov 8, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896421

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.