ClearanceBrief
510(k) K121800 ยท MUH System, X-Ray, Extraoral Source, Digital

POINT 500 HD POINT500C HD

ApplicantPointnix Co., Ltd., Great Neck NY, US
DecisionSubstantially Equivalent, Jan 24, 2013
ReceivedJun 19, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121800

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.