K-number	K053412
Device name	FLEXISCOPE, MODELS 50MH AND 50 MHC
Applicant	Schoelly Imaging, Inc.
Product code	FWF
Device class	Class I
Decision date	Feb 23, 2006
Decision	Substantially Equivalent
Regulation	878.4160

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Source

View the full FDA submission: accessdata.fda.gov

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FLEXISCOPE, MODELS 50MH AND 50 MHC

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