ClearanceBrief
510(k) K770335 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic

COLLIMATOR, AUTOMATIC

ApplicantLitton Medical Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Feb 28, 1977
ReceivedFeb 18, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770335

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.