ClearanceBrief
510(k) K013483 ยท KOD Catheter, Urological

INCARE ADVANCE; INTERMITTENT CATHETER, PLUS INTERMITTENT CATHETER, PLUS KIT

ApplicantHollister, Inc., Libertyville IL, US
DecisionSubstantially Equivalent, Jan 14, 2002
ReceivedOct 19, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013483

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.