ClearanceBrief
510(k) K870429 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

EUSEK-BUSH IN-BATH FILMING DEVICE (#MC-00186)

ApplicantThe Mason Clinic, Seattle WA, US
DecisionSubstantially Equivalent, Feb 11, 1987
ReceivedFeb 5, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870429

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.