510(k) K222010 · DQA Oximeter

Biobeat Platform-2 and BB-613WP Patch

Applicant	Biobeat Technologies , Ltd., Petah Tikvah, IL
Decision	Substantially Equivalent, Dec 30, 2022
Received	Jul 7, 2022
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K222010

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.