K-number	K180709
Device name	truSculpt RF Device; truSculpt; truSculpt 3D
Applicant	Cutera, Inc.
Product code	PBX
Device class	Class II
Decision date	Jun 6, 2018
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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truSculpt RF Device; truSculpt; truSculpt 3D

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