ClearanceBrief
510(k) K952082 ยท EXJ Device, Incontinence, Urosheath Type, Sterile

ROCHESTER MEDICAL CORPORATION SILICONE MALE EXTERNAL CATHETER

ApplicantRochester Medical Corp., Stewartville MN, US
DecisionSubstantially Equivalent, Jul 18, 1995
ReceivedMay 3, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952082

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.