K-number	K211887
Device name	Personal Kinetigraph (PKG) System Gen 2 Plus
Applicant	Gkc Manufacturing Pty, Ltd.
Product code	GYD
Device class	Class II
Decision date	Mar 11, 2022
Decision	Substantially Equivalent
Regulation	882.1950

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View the full FDA submission: accessdata.fda.gov

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Personal Kinetigraph (PKG) System Gen 2 Plus

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