COOLTOUCH ND:YAG LASER SYSTEMS, MODELS CT3S AND CTEV
K-Number: K051434 · 2005-08-09
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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