K-number	K171186
Device name	Cerebrotech CMS-5000
Applicant	Cerebrotech Medical Systems
Product code	QAF
Device class	Class II
Decision date	Dec 8, 2017
Decision	Substantially Equivalent
Regulation	870.2770

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Source

View the full FDA submission: accessdata.fda.gov

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Cerebrotech CMS-5000

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