K-number	K790454
Device name	MODEL 78801A PATIENT MONITORS
Applicant	Hewlett-Packard Co.
Product code	DRT
Device class	Class II
Decision date	Apr 3, 1979
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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MODEL 78801A PATIENT MONITORS

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