K-number	K190542
Device name	Soliton Acoustic Wave Device
Applicant	Soliton, Inc.
Product code	GEX
Device class	Class II
Decision date	May 24, 2019
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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Soliton Acoustic Wave Device

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