ClearanceBrief
510(k) K070911 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

STD MED PRIMO PORT

ApplicantStd Med, Inc., Ayer MA, US
DecisionSubstantially Equivalent, Aug 10, 2007
ReceivedApr 2, 2007
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K070911

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.