ClearanceBrief
510(k) K924164 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

DIGITAL DISK RECORDER W/DUALPATH ARCHIVE/30-60 OPT

ApplicantEigen, Nevada City CA, US
DecisionSubstantially Equivalent, Nov 23, 1992
ReceivedAug 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924164

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.