K-number	K131902
Device name	PENTAX VIDEO UPPER G.I. SCOPES (EG FAMILY)
Applicant	Pentax Medical Company
Product code	FDS
Device class	Class II
Decision date	Apr 10, 2014
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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PENTAX VIDEO UPPER G.I. SCOPES (EG FAMILY)

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