K-number	K820778
Device name	RESPIRATION MONITOR 1000
Applicant	Intl. Medical Devices , Ltd.
Product code	BZQ
Device class	Class II
Decision date	May 3, 1982
Decision	Substantially Equivalent
Regulation	868.2375

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Source

View the full FDA submission: accessdata.fda.gov

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RESPIRATION MONITOR 1000

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