SHARPLAN 723 CO2 LASER SURGICAL SYSTEM
K-Number: K801624 · 1980-08-20
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Device Summary
Frequently Asked Questions
What is the SHARPLAN 723 CO2 LASER SURGICAL SYSTEM?
SHARPLAN 723 CO2 LASER SURGICAL SYSTEM is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Laser Industries , Ltd.. The 510(k) number is K801624.
When did SHARPLAN 723 CO2 LASER SURGICAL SYSTEM receive FDA 510(k) clearance?
SHARPLAN 723 CO2 LASER SURGICAL SYSTEM received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801624.
Who is the listed applicant for SHARPLAN 723 CO2 LASER SURGICAL SYSTEM?
The FDA 510(k) record lists Laser Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHARPLAN 723 CO2 LASER SURGICAL SYSTEM?
The FDA product code for SHARPLAN 723 CO2 LASER SURGICAL SYSTEM 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 Laser Industries , Ltd. 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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