K-number	K201308
Device name	Axonpen, Axonmonitor, Axonbox, Tablet
Applicant	Clearmind Biomedical
Product code	GWG
Device class	Class II
Decision date	Nov 27, 2020
Decision	Substantially Equivalent
Regulation	882.1480

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Source

View the full FDA submission: accessdata.fda.gov

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Axonpen, Axonmonitor, Axonbox, Tablet

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