ClearanceBrief
510(k) K923471 ยท IZH System, X-Ray, Mammographic

PLANMED CYTOGUIDE

ApplicantPlanmed OY, Helsinki, FI
DecisionSubstantially Equivalent, Nov 24, 1992
ReceivedJul 14, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923471

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.