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FDA 510(k)

Photon, Photon Plus

K-Number: K162114 · 2016-12-12

Decision Date2016-12-12
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Photon, Photon Plus is a medical device manufactured by Zolar Technology & Mfg Co., Inc.. It received FDA 510(k) clearance on 2016-12-12 under approval number K162114. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Photon, Photon Plus?

Photon, Photon Plus is a medical device that received FDA 510(k) clearance on 2016-12-12. It is manufactured by Zolar Technology & Mfg Co., Inc.. The 510(k) number is K162114.

When was Photon, Photon Plus approved by the FDA?

Photon, Photon Plus received FDA 510(k) clearance on 2016-12-12, under approval number K162114.

What company makes Photon, Photon Plus?

Photon, Photon Plus is manufactured by Zolar Technology & Mfg Co., Inc..

What is the FDA product code for Photon, Photon Plus?

The FDA product code for Photon, Photon Plus is GEX. This falls under the Gastroenterology category.

Related Devices (Code: GEX)

Official Source

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