K-number	K890606
Device name	OHMEDA 5330 AGENT MONITOR
Applicant	Ohmeda Medical
Product code	CBQ
Device class	Class II
Decision date	Apr 20, 1989
Decision	Substantially Equivalent
Regulation	868.1500

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View the full FDA submission: accessdata.fda.gov

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OHMEDA 5330 AGENT MONITOR

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