K-number	K101898
Device name	R4 ACERT ULTRASOUND REPORTING SYSTEM
Applicant	R4, LLC
Product code	LLZ
Device class	Class II
Decision date	Sep 15, 2011
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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R4 ACERT ULTRASOUND REPORTING SYSTEM

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