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FDA 510(k)

ADVANCED LASER MULTILINE SYSTEM, ALY

K-Number: K952796 · 1995-09-18

ApplicantAdvanced Laser Services Corp.
Decision Date1995-09-18
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADVANCED LASER MULTILINE SYSTEM, ALY is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Laser Services Corp.. It received FDA 510(k) clearance on 1995-09-18 under 510(k) number K952796. 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 ADVANCED LASER MULTILINE SYSTEM, ALY?

ADVANCED LASER MULTILINE SYSTEM, ALY is a medical device that received FDA 510(k) clearance on 1995-09-18. The listed applicant is Advanced Laser Services Corp.. The 510(k) number is K952796.

When did ADVANCED LASER MULTILINE SYSTEM, ALY receive FDA 510(k) clearance?

ADVANCED LASER MULTILINE SYSTEM, ALY received FDA 510(k) clearance on 1995-09-18, under 510(k) number K952796.

Who is the listed applicant for ADVANCED LASER MULTILINE SYSTEM, ALY?

The FDA 510(k) record lists Advanced Laser Services Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADVANCED LASER MULTILINE SYSTEM, ALY?

The FDA product code for ADVANCED LASER MULTILINE SYSTEM, ALY is GEX. This falls under the Gastroenterology category.

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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.

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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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