K-number	K181199
Device name	Katalyst Mark 1 Muscle Stimulation System Model 2
Applicant	Katalyst, Inc.
Product code	NGX
Device class	Class II
Decision date	Sep 20, 2018
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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Katalyst Mark 1 Muscle Stimulation System Model 2

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