K-number	K812041
Device name	VENTI-MONITOR MODEL 101
Applicant	Medix Medical Electronics (U.S.A.), Inc.
Product code	CAP
Device class	Class II
Decision date	Sep 25, 1981
Decision	Substantially Equivalent
Regulation	868.2600

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View the full FDA submission: accessdata.fda.gov

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VENTI-MONITOR MODEL 101

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