K-number	K161628
Device name	JAS Pulse(TM) Ultrasonic Therapy
Applicant	Bonutti Research, Inc.
Product code	IMI
Device class	Class II
Decision date	Nov 10, 2016
Decision	Substantially Equivalent
Regulation	890.5300

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View the full FDA submission: accessdata.fda.gov

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JAS Pulse(TM) Ultrasonic Therapy

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