K-number	K132804
Device name	ACUSON S1000 / S2000 / S3000
Applicant	Siemens Medical Solutions USA, Inc. Ultrasound Gro
Product code	IYN
Device class	Class II
Decision date	Oct 24, 2013
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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ACUSON S1000 / S2000 / S3000

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