ClearanceBrief
510(k) K082126 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

RHAPSODY MRI

ApplicantGrantadler Corporation, Appollo Beach FL, US
DecisionSubstantially Equivalent, Nov 13, 2008
ReceivedJul 29, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082126

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.