K-number	K792573
Device name	ALARM USED W/MONITORING SPIROMETER
Applicant	Empire Plastics Manufacturer
Product code	BZK
Device class	Class II
Decision date	Dec 31, 1979
Decision	Substantially Equivalent
Regulation	868.1850

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Source

View the full FDA submission: accessdata.fda.gov

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ALARM USED W/MONITORING SPIROMETER

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