ClearanceBrief
510(k) K151772 ยท GBM Catheter, Urethral

Actreen Mini Intermittent Urinary Catheters

ApplicantB.Braun Medical, Inc., Allentown PA, US
DecisionSubstantially Equivalent, Feb 9, 2016
ReceivedJun 30, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K151772

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.