K-number	K211720
Device name	Planmed Clarity 2D, Planmed Clarify S
Applicant	Planmed OY
Product code	MUE
Device class	Class II
Decision date	Jul 18, 2022
Decision	Substantially Equivalent
Regulation	892.1715

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Source

View the full FDA submission: accessdata.fda.gov

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Planmed Clarity 2D, Planmed Clarify S

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