K-number	K923273
Device name	AI 5200 DIAGNOSTIC ULTRASOUND SYSTEM
Applicant	Acoustic Imaging Technologies Corp.
Product code	IYO
Device class	Class II
Decision date	Dec 27, 1994
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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AI 5200 DIAGNOSTIC ULTRASOUND SYSTEM

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