K-number	K210607
Device name	PALACOS R pro, PALACOS R+G pro, PALACOS MV+G pro
Applicant	Heraeus Medical GmbH
Product code	LOD
Device class	Class II
Decision date	Jul 9, 2021
Decision	Substantially Equivalent
Regulation	888.3027

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Source

View the full FDA submission: accessdata.fda.gov

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PALACOS R pro, PALACOS R+G pro, PALACOS MV+G pro

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