ClearanceBrief
510(k) K120318 ยท MUH System, X-Ray, Extraoral Source, Digital

VIVI ERGON-X HF

ApplicantVivi S.R.L., Imoa, IT
DecisionSubstantially Equivalent, Mar 6, 2012
ReceivedFeb 2, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120318

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.