K-number	K003222
Device name	MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER
Applicant	Computer Motion, Inc.
Product code	GCI
Device class	Class II
Decision date	Nov 3, 2000
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER

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