ClearanceBrief
510(k) K963265 ยท EXJ Device, Incontinence, Urosheath Type, Sterile

PROSYS SAMEC LA

ApplicantConvatec, A Division of E.R. Squibb & Sons, Skillman NJ, US
DecisionSubstantially Equivalent, Oct 25, 1996
ReceivedAug 20, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963265

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.