510(k) K212153 ยท DQA Oximeter
Biobeat Platform, BB-613WP Patch
| Applicant | Biobeat Technologies , Ltd., Petah Tikvah, IL |
| Decision | Substantially Equivalent, Mar 25, 2022 |
| Received | Jul 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212153
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.