ClearanceBrief
510(k) K952392 ยท FPA Set, Administration, Intravascular

MLI SET

ApplicantMedical Technologies of Georgia, Decatur GA, US
DecisionSubstantially Equivalent, Aug 7, 1995
ReceivedMay 22, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952392

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.