MODEL SL45 SURGILASE CO2 SURGICAL LASER SYSTEMS
K-Number: K884313 · 1988-10-27
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Device Summary
Frequently Asked Questions
What is the MODEL SL45 SURGILASE CO2 SURGICAL LASER SYSTEMS?
MODEL SL45 SURGILASE CO2 SURGICAL LASER SYSTEMS is a medical device that received FDA 510(k) clearance on 1988-10-27. The listed applicant is Surgilase, Inc.. The 510(k) number is K884313.
When did MODEL SL45 SURGILASE CO2 SURGICAL LASER SYSTEMS receive FDA 510(k) clearance?
MODEL SL45 SURGILASE CO2 SURGICAL LASER SYSTEMS received FDA 510(k) clearance on 1988-10-27, under 510(k) number K884313.
Who is the listed applicant for MODEL SL45 SURGILASE CO2 SURGICAL LASER SYSTEMS?
The FDA 510(k) record lists Surgilase, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL SL45 SURGILASE CO2 SURGICAL LASER SYSTEMS?
The FDA product code for MODEL SL45 SURGILASE CO2 SURGICAL LASER SYSTEMS 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 Surgilase, 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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