K-number	K940681
Device name	CLEARVIEW UTERINE MANIPULATOR
Applicant	Clinical Innovations, Inc.
Product code	LKF
Device class	Class II
Decision date	Jul 26, 1994
Decision	Substantially Equivalent
Regulation	884.4530

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View the full FDA submission: accessdata.fda.gov

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CLEARVIEW UTERINE MANIPULATOR

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