K-number	K170813
Device name	ORTHOPANTOMOGRAPH OP 3D
Applicant	Palodex Group OY
Product code	OAS
Device class	Class II
Decision date	Apr 7, 2017
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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ORTHOPANTOMOGRAPH OP 3D

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