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FDA 510(k)

NOABLE LASER

K-Number: K242207 · 2025-03-07

Decision Date2025-03-07
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NOABLE LASER is a medical device manufactured by Daeju Meditech Engineering Co., Ltd.. It received FDA 510(k) clearance on 2025-03-07 under approval number K242207. 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 NOABLE LASER?

NOABLE LASER is a medical device that received FDA 510(k) clearance on 2025-03-07. It is manufactured by Daeju Meditech Engineering Co., Ltd.. The 510(k) number is K242207.

When was NOABLE LASER approved by the FDA?

NOABLE LASER received FDA 510(k) clearance on 2025-03-07, under approval number K242207.

What company makes NOABLE LASER?

NOABLE LASER is manufactured by Daeju Meditech Engineering Co., Ltd..

What is the FDA product code for NOABLE LASER?

The FDA product code for NOABLE LASER is GEX. This falls under the Gastroenterology category.

Other Devices by Daeju Meditech Engineering Co., Ltd.

Related Devices (Code: GEX)

Official Source

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