K-number	K081004
Device name	PROTECTISCOPE CS COLONOSCOPE, NON-INTRAPULL
Applicant	Stryker GI
Product code	FDF
Device class	Class II
Decision date	May 2, 2008
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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PROTECTISCOPE CS COLONOSCOPE, NON-INTRAPULL

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