K-number	K060899
Device name	FLEXILUX II CYSTOSCOPE AND HYSTEROSCOPE
Applicant	Schoelly Imaging, Inc.
Product code	FAJ
Device class	Class II
Decision date	Mar 2, 2007
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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FLEXILUX II CYSTOSCOPE AND HYSTEROSCOPE

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