K-number	K131096
Device name	AR1000 SERIES ULTRASONIC WOUND THERAPY SYSTEM
Applicant	Arobella Medical, LLC
Product code	NRB
Device class	Class II
Decision date	May 16, 2014
Decision	Substantially Equivalent
Regulation	878.4410

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View the full FDA submission: accessdata.fda.gov

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AR1000 SERIES ULTRASONIC WOUND THERAPY SYSTEM

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