K-number	K173371
Device name	VisuMax Femtosecond Laser
Applicant	Carl Zeiss Meditec, Inc.
Product code	HNO
Device class	Class I
Decision date	Apr 13, 2018
Decision	Substantially Equivalent
Regulation	886.4370

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Source

View the full FDA submission: accessdata.fda.gov

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VisuMax Femtosecond Laser

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