K-number	K954129
Device name	SPECTRADIGITAL SERIES V250DSP
Applicant	Hitachi Medical Corp. of America
Product code	KPS
Device class	Class II
Decision date	Dec 22, 1995
Decision	Substantially Equivalent
Regulation	892.1200

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View the full FDA submission: accessdata.fda.gov

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SPECTRADIGITAL SERIES V250DSP

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