SURGILASE YAG 100 SURGICAL LASER SYSTEM
K-Number: K902211 · 1990-06-29
Advertisement
Device Summary
Frequently Asked Questions
What is the SURGILASE YAG 100 SURGICAL LASER SYSTEM?
SURGILASE YAG 100 SURGICAL LASER SYSTEM is a medical device that received FDA 510(k) clearance on 1990-06-29. The listed applicant is Surgilase, Inc.. The 510(k) number is K902211.
When did SURGILASE YAG 100 SURGICAL LASER SYSTEM receive FDA 510(k) clearance?
SURGILASE YAG 100 SURGICAL LASER SYSTEM received FDA 510(k) clearance on 1990-06-29, under 510(k) number K902211.
Who is the listed applicant for SURGILASE YAG 100 SURGICAL LASER SYSTEM?
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 SURGILASE YAG 100 SURGICAL LASER SYSTEM?
The FDA product code for SURGILASE YAG 100 SURGICAL LASER 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 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.
Advertisement