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FDA 510(k)

LASERSCOPE EL LASER SYSTEM AND ACCESSORIES

K-Number: K974896 · 1998-03-27

ApplicantLaserscope
Decision Date1998-03-27
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LASERSCOPE EL LASER SYSTEM AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Laserscope. It received FDA 510(k) clearance on 1998-03-27 under 510(k) number K974896. 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 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.

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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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