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FDA 510(k)

VIRIDIS LASER

K-Number: K001784 · 2000-09-11

ApplicantCosmos Medical Technology
Decision Date2000-09-11
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VIRIDIS LASER is the device name listed in this FDA 510(k) record. The listed applicant is Cosmos Medical Technology. It received FDA 510(k) clearance on 2000-09-11 under 510(k) number K001784. 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 VIRIDIS LASER?

VIRIDIS LASER is a medical device that received FDA 510(k) clearance on 2000-09-11. The listed applicant is Cosmos Medical Technology. The 510(k) number is K001784.

When did VIRIDIS LASER receive FDA 510(k) clearance?

VIRIDIS LASER received FDA 510(k) clearance on 2000-09-11, under 510(k) number K001784.

Who is the listed applicant for VIRIDIS LASER?

The FDA 510(k) record lists Cosmos Medical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIRIDIS LASER?

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

Related Clinical Trials

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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Other records listing Cosmos Medical Technology as applicant

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.

K001704ATHOSK983020COMPACT KTP LASER

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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