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FDA 510(k)

Holmium Medical Laser

K-Number: K231718 · 2023-08-18

Decision Date2023-08-18
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Holmium Medical Laser is a medical device manufactured by Allengers Global Healthcare Private Limited. It received FDA 510(k) clearance on 2023-08-18 under approval number K231718. 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 Holmium Medical Laser?

Holmium Medical Laser is a medical device that received FDA 510(k) clearance on 2023-08-18. It is manufactured by Allengers Global Healthcare Private Limited. The 510(k) number is K231718.

When was Holmium Medical Laser approved by the FDA?

Holmium Medical Laser received FDA 510(k) clearance on 2023-08-18, under approval number K231718.

What company makes Holmium Medical Laser?

Holmium Medical Laser is manufactured by Allengers Global Healthcare Private Limited.

What is the FDA product code for Holmium Medical Laser?

The FDA product code for Holmium Medical Laser is GEX. This falls under the Gastroenterology category.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.