K-number	K812167
Device name	MODEL 78850 OXYGEN MONITOR
Applicant	Hewlett-Packard Co.
Product code	KLK
Device class	Class II
Decision date	Aug 31, 1981
Decision	Substantially Equivalent
Regulation	868.2500

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View the full FDA submission: accessdata.fda.gov

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MODEL 78850 OXYGEN MONITOR

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