ClearanceBrief
510(k) K950690 ยท EXJ Device, Incontinence, Urosheath Type, Sterile

PROSYS URIHESICE SYSTEM NL

ApplicantConvatec, A Division of E.R. Squibb & Sons, Skillman NJ, US
DecisionSubstantially Equivalent, Mar 23, 1995
ReceivedFeb 14, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950690

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.