ClearanceBrief
510(k) K071423 ยท EZL Catheter, Retention Type, Balloon

MEDLINE LATEX FOLEY CATHETER

ApplicantMedline Industries, Inc., Mundelein IL, US
DecisionSubstantially Equivalent, Jul 18, 2007
ReceivedMay 22, 2007
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K071423

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.