ClearanceBrief
510(k) K923533 ยท JAC System, X-Ray, Film Marking, Radiographic

ADMARK

ApplicantPlanmeca USA, Inc., Finland, FI
DecisionSubstantially Equivalent, Mar 4, 1993
ReceivedJul 16, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923533

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.