ClearanceBrief
510(k) K904044 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic

TF-63SA

ApplicantToshiba America Medical Systems, In.C, Tustin CA, US
DecisionSubstantially Equivalent, Nov 29, 1990
ReceivedSep 4, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904044

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.