ClearanceBrief
510(k) K837304 ยท

MODELS 246 AND 210F LINEAR ARRAY ULTRASOUND SCANNER

ApplicantAloka Co., Ltd., Tokyo, JP
DecisionSubstantially Equivalent, May 9, 1983
ReceivedMar 18, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K837304

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.