ClearanceBrief
510(k) K971796 ยท EZL Catheter, Retention Type, Balloon

LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS

ApplicantLouisville Laboratories, Inc., North Attleboro MA, US
DecisionSubstantially Equivalent, Aug 12, 1997
ReceivedMay 15, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K971796

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.