ClearanceBrief
510(k) K935630 ยท EZL Catheter, Retention Type, Balloon

NORTA

ApplicantBeiersdorf, Inc., Norwalk CT, US
DecisionSubstantially Equivalent, Oct 7, 1994
ReceivedNov 23, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935630

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.