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FDA 510(k)

PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes

K-Number: K173679 · 2018-07-03

Decision Date2018-07-03
Product CodePEA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is a medical device manufactured by Pentax of America, Inc.. It received FDA 510(k) clearance on 2018-07-03 under approval number K173679. The device is classified under product code PEA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?

PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is a medical device that received FDA 510(k) clearance on 2018-07-03. It is manufactured by Pentax of America, Inc.. The 510(k) number is K173679.

When was PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes approved by the FDA?

PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes received FDA 510(k) clearance on 2018-07-03, under approval number K173679.

What company makes PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?

PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is manufactured by Pentax of America, Inc..

What is the FDA product code for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?

The FDA product code for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is PEA.

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Official Source

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