ClearanceBrief
510(k) K030120 ยท EZL Catheter, Retention Type, Balloon

AMSURE FOLEY CATHETER

ApplicantAmsino International, Inc., Ontario CA, US
DecisionSubstantially Equivalent, Oct 29, 2003
ReceivedJan 13, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030120

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.