ClearanceBrief
510(k) K003784 ยท EZL Catheter, Retention Type, Balloon

MENTOR SELF-CATH PLUS

ApplicantMentor Corp., Santa Barbara CA, US
DecisionSubstantially Equivalent, Mar 5, 2001
ReceivedDec 7, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003784

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.