ClearanceBrief
510(k) K875233 ยท IXC Illuminator, Radiographic-Film

VARIVIEWER (X-RAY FILM VIEWER)

ApplicantDiversified Diagnostic Products, Inc., Houston TX, US
DecisionSubstantially Equivalent, Jan 19, 1988
ReceivedDec 22, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K875233

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.