ClearanceBrief
510(k) K827284 ยท

MODEL SSD-119

ApplicantAloka Co., Ltd., Walker MI, US
DecisionSubstantially Equivalent, Apr 21, 1982
ReceivedMar 30, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K827284

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.