K-number	K012253
Device name	SSD-1000 DIAGNOSTIC ULTRASOUND SYSTEM
Applicant	Aloka Co., Ltd.
Product code	IYO
Device class	Class II
Decision date	Aug 30, 2001
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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SSD-1000 DIAGNOSTIC ULTRASOUND SYSTEM

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