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Biobeat Technologies , Ltd.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories2
Latest FDA decision2025-01-14
TypeNumberDevice NameCodeDateActions
510(k) K241066 BB-613-BPMDXN2025-01-14 View
510(k) K222010 Biobeat Platform-2 and BB-613WP PatchDQA2022-12-30 View
510(k) K212153 Biobeat Platform, BB-613WP PatchDQA2022-03-25 View
510(k) K190792 BB-613WPDQA2019-08-22 View

Related Clinical Trials

NCT07240831Accuracy of a Cuffless Photoplethysmography (PPG) Chest-Patch Monitor for 24-hour Ambulatory Blood Pressure Monitoring (ABPM)RECRUITING
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