K-number	K201332
Device name	Meditech ABPM-06 (BP6)
Applicant	Meditech , Ltd.
Product code	DXN
Device class	Class II
Decision date	Feb 10, 2021
Decision	Substantially Equivalent
Regulation	870.1130

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View the full FDA submission: accessdata.fda.gov

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Meditech ABPM-06 (BP6)

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