ClearanceBrief
510(k) K900935 ยท LMD System, Digital Image Communications, Radiological

DU PONT LINX LASER IMAGER W/THE LINX NETWORKING

ApplicantE.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US
DecisionSubstantially Equivalent, May 15, 1990
ReceivedFeb 28, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900935

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.