ClearanceBrief
510(k) K190792 ยท DQA Oximeter

BB-613WP

ApplicantBiobeat Technologies , Ltd., Petah Tikvah, IL
DecisionSubstantially Equivalent, Aug 22, 2019
ReceivedMar 27, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190792

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.