K-number	K893216
Device name	RMI ULTRASOUND DOPPLER PHANTOM SYSTEM
Applicant	Radiation Measurements, Inc.
Product code	GXX
Device class	Class I
Decision date	Sep 5, 1989
Decision	Substantially Equivalent
Regulation	882.1925

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View the full FDA submission: accessdata.fda.gov

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RMI ULTRASOUND DOPPLER PHANTOM SYSTEM

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