SHARPLAN CO2 SURGICAL LASER
K-Number: K933362 · 1994-04-07
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Device Summary
Frequently Asked Questions
What is the SHARPLAN CO2 SURGICAL LASER?
SHARPLAN CO2 SURGICAL LASER is a medical device that received FDA 510(k) clearance on 1994-04-07. The listed applicant is Laser Industries , Ltd.. The 510(k) number is K933362.
When did SHARPLAN CO2 SURGICAL LASER receive FDA 510(k) clearance?
SHARPLAN CO2 SURGICAL LASER received FDA 510(k) clearance on 1994-04-07, under 510(k) number K933362.
Who is the listed applicant for SHARPLAN CO2 SURGICAL LASER?
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 CO2 SURGICAL LASER?
The FDA product code for SHARPLAN CO2 SURGICAL LASER 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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