K-number	K222010
Device name	Biobeat Platform-2 and BB-613WP Patch
Applicant	Biobeat Technologies , Ltd.
Product code	DQA
Device class	Class II
Decision date	Dec 30, 2022
Decision	Substantially Equivalent
Regulation	870.2700

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Source

View the full FDA submission: accessdata.fda.gov

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Biobeat Platform-2 and BB-613WP Patch

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