ClearanceBrief
510(k) K926348 ยท LMB Device, Digital Image Storage, Radiological

SC1000 SCAN CONVERTER

ApplicantPerkins Mfg. Co., Dallas TX, US
DecisionSubstantially Equivalent, Nov 19, 1993
ReceivedDec 17, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926348

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.