K-number	K881420
Device name	OMNI-VENT, SERIES D/MRI
Applicant	Stein-Gates Medical Equipment, Inc.
Product code	CBK
Device class	Class II
Decision date	Jun 14, 1988
Decision	Substantially Equivalent
Regulation	868.5895

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View the full FDA submission: accessdata.fda.gov

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OMNI-VENT, SERIES D/MRI

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