K-number	K122470
Device name	PENTAX EPK-I5010 VIDEO PROCESSOR
Applicant	Pentax Medical
Product code	PEA
Device class	Class II
Decision date	Apr 10, 2013
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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PENTAX EPK-I5010 VIDEO PROCESSOR

Everything you need for a 510(k) submission. Nothing you don't.