K-number	K872178
Device name	MODIFICATION TO ARKIVE(TM)
Applicant	Diatek, Inc.
Product code	BSZ
Device class	Class II
Decision date	Jan 27, 1988
Decision	Substantially Equivalent
Regulation	868.5160

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO ARKIVE(TM)

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