K-number	K102663
Device name	AED RESECTOSCOPE
Applicant	National Advanced Endoscopy Devices, Inc.
Product code	FJL
Device class	Class II
Decision date	Dec 30, 2010
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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AED RESECTOSCOPE

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