K-number	K870783
Device name	BPA CARDIOVASCULAR PRESSURE AMPLIFIER
Applicant	Fisher Imaging Corp.
Product code	DRQ
Device class	Class II
Decision date	Apr 27, 1987
Decision	Substantially Equivalent
Regulation	870.2060

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View the full FDA submission: accessdata.fda.gov

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BPA CARDIOVASCULAR PRESSURE AMPLIFIER

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