ClearanceBrief
510(k) K924249 ยท KMK Device, Intravascular Catheter Securement

DERMASSIST TRANSPARENT SITE DRESSING

ApplicantWilshire Medical Products, Dallas TX, US
DecisionSubstantially Equivalent, Feb 3, 1993
ReceivedAug 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924249

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.