K-number	K061627
Device name	MODIFICATION TO I VENT 201
Applicant	Versamed Medical Systems, Inc.
Product code	CBK
Device class	Class II
Decision date	Jun 29, 2006
Decision	Substantially Equivalent
Regulation	868.5895

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO I VENT 201

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