ClearanceBrief
510(k) K092329 ยท MUH System, X-Ray, Extraoral Source, Digital

SOPIX 2

ApplicantSopro, Mt. Laurel NJ, US
DecisionSubstantially Equivalent, Jul 20, 2010
ReceivedAug 4, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092329

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.