![](/images/devices/Biobeat/BB-613WP-chest.jpg)
Accuracy Assessment | Recommendation | Basis | |
BP | Medaval | None | Although equivalence to another device is claimed, this has not been tested to MDR requirements. |
BP | FDA (US) | 510(k) | 510(k) K190792 |
Legend: F FDA 510(k)
Note: This is a provisional list, as equivalence according to EU Regulation 2017/745 (e.g. MEDDEV 2.7/1 rev 4) is not proven. Accordingly, these publications are not used in the assessment of star-ratings.
Biobeat BB-613 Wrist Watch
Eisenkraft A, Nachman D. Human study of the Biobeat device allowing for non-invasive wireless continuous measurement of blood pressure. (US) Military Health System Research Symposium 2018. Epub: 2018 Sep. doi: 10.13140/RG.2.2.16570.03527. Available from: www.biobeat.cloud. Poster presentation.
Ad Hoc protocol General population (Note: ESH-IP 2010 criteria applied to sample for which it may not be applicable)
The results of the study have only been published in poster form and their validity cannot be verified.
Biobeat BB-613WP (Wrist-monitor)
Nachman D, Gepner Y, Goldstein N, Kabakov E, Ishay AB, Littman R, Azmon Y, Jaffe E, Eisenkraft A. Comparing blood pressure measurements between a photoplethysmography-based and a standard cuff-based manometry device. Sci Rep.;10:16116. Epub: 2020 Sep 30. doi: 10.1038/s41598-020-73172-3.
Ad Hoc protocol General population (Note: Partial ISO 81060-2:2013 criteria applied to large sample but for which BP and other distribution requirements are not provided.)