SHARPLAN FLEXIBLE CO2 SURGICAL LASER APPLICATOR
K-Number: K900076 · 1990-03-22
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Device Summary
Frequently Asked Questions
What is the SHARPLAN FLEXIBLE CO2 SURGICAL LASER APPLICATOR?
SHARPLAN FLEXIBLE CO2 SURGICAL LASER APPLICATOR is a medical device that received FDA 510(k) clearance on 1990-03-22. The listed applicant is Sharplan Lasers, Inc.. The 510(k) number is K900076.
When did SHARPLAN FLEXIBLE CO2 SURGICAL LASER APPLICATOR receive FDA 510(k) clearance?
SHARPLAN FLEXIBLE CO2 SURGICAL LASER APPLICATOR received FDA 510(k) clearance on 1990-03-22, under 510(k) number K900076.
Who is the listed applicant for SHARPLAN FLEXIBLE CO2 SURGICAL LASER APPLICATOR?
The FDA 510(k) record lists Sharplan Lasers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHARPLAN FLEXIBLE CO2 SURGICAL LASER APPLICATOR?
The FDA product code for SHARPLAN FLEXIBLE CO2 SURGICAL LASER APPLICATOR 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 Sharplan Lasers, Inc. 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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