K-number	K210902
Device name	EliA Ro52, EliA Ro60
Applicant	Phadia AB
Product code	LKJ
Device class	Class II
Decision date	Jul 27, 2022
Decision	Substantially Equivalent
Regulation	866.5100

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Source

View the full FDA submission: accessdata.fda.gov

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EliA Ro52, EliA Ro60

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