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FDA 510(k)

Alma Diode Tabletop Laser

K-Number: K160952 · 2016-05-05

ApplicantAlma, Ltd.
Decision Date2016-05-05
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Alma Diode Tabletop Laser is the device name listed in this FDA 510(k) record. The listed applicant is Alma, Ltd.. It received FDA 510(k) clearance on 2016-05-05 under 510(k) number K160952. 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 Alma Diode Tabletop Laser?

Alma Diode Tabletop Laser is a medical device that received FDA 510(k) clearance on 2016-05-05. The listed applicant is Alma, Ltd.. The 510(k) number is K160952.

When did Alma Diode Tabletop Laser receive FDA 510(k) clearance?

Alma Diode Tabletop Laser received FDA 510(k) clearance on 2016-05-05, under 510(k) number K160952.

Who is the listed applicant for Alma Diode Tabletop Laser?

The FDA 510(k) record lists Alma, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Alma Diode Tabletop Laser?

The FDA product code for Alma Diode Tabletop Laser is GEX. This falls under the Gastroenterology category.

Related Devices (Code: GEX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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