K-number	K160506
Device name	Planmeca ProMax 3D Max, Planmeca Maximity
Applicant	Planmeca Oy
Product code	OAS
Device class	Class II
Decision date	May 20, 2016
Decision	Substantially Equivalent
Regulation	892.1750

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View the full FDA submission: accessdata.fda.gov

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Planmeca ProMax 3D Max, Planmeca Maximity

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