K-number	K170215
Device name	LaserDock, HolmiumDock, CO2Dock,OmniDock, KTPDock
Applicant	Patient Pocket, LLC
Product code	GEX
Device class	Class II
Decision date	Apr 19, 2017
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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LaserDock, HolmiumDock, CO2Dock,OmniDock, KTPDock

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