K-number	K983732
Device name	THORAX FD AND MULTIX FD
Applicant	Siemens Medical Solutions USA, Inc.
Product code	MQB
Device class	Class II
Decision date	Apr 21, 1999
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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THORAX FD AND MULTIX FD

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