K-number	K130978
Device name	ZTX ULTRASONIC DIATHERMY DEVICE
Applicant	Zetroz, Inc.
Product code	PFW
Device class	Class II
Decision date	Nov 6, 2013
Decision	Substantially Equivalent
Regulation	890.5300

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Source

View the full FDA submission: accessdata.fda.gov

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ZTX ULTRASONIC DIATHERMY DEVICE

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