ClearanceBrief
510(k) K772144 ยท EXJ Device, Incontinence, Urosheath Type, Sterile

CATHETER, DISP., EXTERNAL, MALE

ApplicantMedline Industries, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 28, 1977
ReceivedNov 15, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772144

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.