K-number	K191846
Device name	MAXReach Laser Probe
Applicant	Vortex Surgical, Inc.
Product code	HQB
Device class	Class II
Decision date	Dec 23, 2019
Decision	Substantially Equivalent
Regulation	886.4690

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Source

View the full FDA submission: accessdata.fda.gov

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MAXReach Laser Probe

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