ClearanceBrief
510(k) K945752 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

CELSITE(TM) BRACHIAL VENOUS PORT

ApplicantB. Braun of America, Inc., Bethlehem PA, US
DecisionSubstantially Equivalent, May 31, 1995
ReceivedNov 23, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945752

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.