K-number	K212938
Device name	Vitalograph Model 6000 Alpha
Applicant	Vitalograph Ireland, Ltd.
Product code	BZG
Device class	Class II
Decision date	Jan 26, 2022
Decision	Substantially Equivalent
Regulation	868.1840

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Source

View the full FDA submission: accessdata.fda.gov

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Vitalograph Model 6000 Alpha

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