K-number	K233804
Device name	Resonic Rapid Acoustic Pulse Device
Applicant	Zeltiq Aesthetics, Inc.
Product code	GEX
Device class	Class II
Decision date	Feb 1, 2024
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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Resonic Rapid Acoustic Pulse Device

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