ClearanceBrief
510(k) K882184 ยท LMB Device, Digital Image Storage, Radiological

HR-1000 W/SUFFIXES (B,C OR D)

ApplicantEigen, Nevada City CA, US
DecisionSubstantially Equivalent, Jun 28, 1988
ReceivedMay 24, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882184

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.