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FDA 510(k)

SURGILASE SL 150 SURGICAL LASER SYSTEM

K-Number: K905006 · 1991-02-21

Decision Date1991-02-21
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGILASE SL 150 SURGICAL LASER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surgilase, Inc.. It received FDA 510(k) clearance on 1991-02-21 under 510(k) number K905006. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGILASE SL 150 SURGICAL LASER SYSTEM?

SURGILASE SL 150 SURGICAL LASER SYSTEM is a medical device that received FDA 510(k) clearance on 1991-02-21. The listed applicant is Surgilase, Inc.. The 510(k) number is K905006.

When did SURGILASE SL 150 SURGICAL LASER SYSTEM receive FDA 510(k) clearance?

SURGILASE SL 150 SURGICAL LASER SYSTEM received FDA 510(k) clearance on 1991-02-21, under 510(k) number K905006.

Who is the listed applicant for SURGILASE SL 150 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 SL 150 SURGICAL LASER SYSTEM?

The FDA product code for SURGILASE SL 150 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.

View all 19 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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