K-number	K843681
Device name	RESPIRATION & HEART RATE MONITOR 530
Applicant	Tri-Med, Inc.
Product code	BZQ
Device class	Class II
Decision date	Dec 4, 1984
Decision	Substantially Equivalent
Regulation	868.2375

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View the full FDA submission: accessdata.fda.gov

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RESPIRATION & HEART RATE MONITOR 530

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