AURA ISURGICAL LASER SYSTEM & ACCESSORIES
K-Number: K024206 · 2003-11-17
Advertisement
Device Summary
Frequently Asked Questions
What is the AURA ISURGICAL LASER SYSTEM & ACCESSORIES?
AURA ISURGICAL LASER SYSTEM & ACCESSORIES is a medical device that received FDA 510(k) clearance on 2003-11-17. The listed applicant is Laserscope. The 510(k) number is K024206.
When did AURA ISURGICAL LASER SYSTEM & ACCESSORIES receive FDA 510(k) clearance?
AURA ISURGICAL LASER SYSTEM & ACCESSORIES received FDA 510(k) clearance on 2003-11-17, under 510(k) number K024206.
Who is the listed applicant for AURA ISURGICAL LASER SYSTEM & 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 AURA ISURGICAL LASER SYSTEM & ACCESSORIES?
The FDA product code for AURA ISURGICAL LASER SYSTEM & 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.
Advertisement