K-number	K770330
Device name	MONITOR, PULSE WAVE VELOCITY P607
Applicant	Cyborg Corp.
Product code	DXG
Device class	Class II
Decision date	Feb 24, 1977
Decision	Substantially Equivalent
Regulation	870.1435

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View the full FDA submission: accessdata.fda.gov

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MONITOR, PULSE WAVE VELOCITY P607

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