K-number	K810177
Device name	PATIENT MONITOR MODEL CM130, 140
Applicant	Honeywell, Inc.
Product code	DXG
Device class	Class II
Decision date	Feb 25, 1981
Decision	Substantially Equivalent
Regulation	870.1435

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View the full FDA submission: accessdata.fda.gov

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PATIENT MONITOR MODEL CM130, 140

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