K-number	K190042
Device name	Brainlab Elements Image Fusion Angio
Applicant	Brainlab AG
Product code	LLZ
Device class	Class II
Decision date	Apr 25, 2019
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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Brainlab Elements Image Fusion Angio

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