K-number	K840469
Device name	TYCOS SELF CHECK BPM3 BLOOD PRESS MONI
Applicant	Sybron Corp.
Product code	DXN
Device class	Class II
Decision date	May 21, 1984
Decision	Substantially Equivalent
Regulation	870.1130

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View the full FDA submission: accessdata.fda.gov

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TYCOS SELF CHECK BPM3 BLOOD PRESS MONI

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