ClearanceBrief
510(k) K942941 ยท EXJ Device, Incontinence, Urosheath Type, Sterile

CONQUEST MALE CONTINENCE SYSTEM

ApplicantConvatec, A Bristol-Myers Squibb Co., Princeton NJ, US
DecisionSubstantially Equivalent, Mar 17, 1995
ReceivedJun 22, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942941

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.