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FDA 510(k)

COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV

K-Number: K051434 · 2005-08-09

Decision Date2005-08-09
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV is the device name listed in this FDA 510(k) record. The listed applicant is New Star Lasers, Inc.. It received FDA 510(k) clearance on 2005-08-09 under 510(k) number K051434. 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 COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV?

COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV is a medical device that received FDA 510(k) clearance on 2005-08-09. The listed applicant is New Star Lasers, Inc.. The 510(k) number is K051434.

When did COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV receive FDA 510(k) clearance?

COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV received FDA 510(k) clearance on 2005-08-09, under 510(k) number K051434.

Who is the listed applicant for COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV?

The FDA 510(k) record lists New Star Lasers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV?

The FDA product code for COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV 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.

Other records listing New Star Lasers, Inc. 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.

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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.

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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