ClearanceBrief
510(k) K827408 ยท

ULTRA IMAGER

ApplicantHoneywell, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Oct 4, 1982
ReceivedJul 28, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K827408

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.