LASERSCOPE EL LASER SYSTEM AND ACCESSORIES
K-Number: K974896 · 1998-03-27
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Device Summary
Frequently Asked Questions
What is the LASERSCOPE EL LASER SYSTEM AND ACCESSORIES?
LASERSCOPE EL LASER SYSTEM AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1998-03-27. The listed applicant is Laserscope. The 510(k) number is K974896.
When did LASERSCOPE EL LASER SYSTEM AND ACCESSORIES receive FDA 510(k) clearance?
LASERSCOPE EL LASER SYSTEM AND ACCESSORIES received FDA 510(k) clearance on 1998-03-27, under 510(k) number K974896.
Who is the listed applicant for LASERSCOPE EL LASER SYSTEM AND ACCESSORIES?
The FDA 510(k) record lists Laserscope as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LASERSCOPE EL LASER SYSTEM AND ACCESSORIES?
The FDA product code for LASERSCOPE EL LASER SYSTEM AND ACCESSORIES 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 Laserscope 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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