Biobeat Technologies , Ltd.

Biobeat Technologies , Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 2019, most recent 2025.

Top product codes for Biobeat Technologies , Ltd.

DQA — Cardiovascular3 devices
DXN — Cardiovascular1 device

Recent clearances by Biobeat Technologies , Ltd.

K241066 — BB-613-BPMCode DXN·2025-01-14
K222010 — Biobeat Platform-2 and BB-613WP PatchCode DQA·2022-12-30
K212153 — Biobeat Platform, BB-613WP PatchCode DQA·2022-03-25
K190792 — BB-613WPCode DQA·2019-08-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.