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FDA 510(k)

RELIANT LASER SYSTEM II

K-Number: K040617 · 2004-06-15

ApplicantReliant Technologies, Inc.
Decision Date2004-06-15
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RELIANT LASER SYSTEM II is the device name listed in this FDA 510(k) record. The listed applicant is Reliant Technologies, Inc.. It received FDA 510(k) clearance on 2004-06-15 under 510(k) number K040617. 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 RELIANT LASER SYSTEM II?

RELIANT LASER SYSTEM II is a medical device that received FDA 510(k) clearance on 2004-06-15. The listed applicant is Reliant Technologies, Inc.. The 510(k) number is K040617.

When did RELIANT LASER SYSTEM II receive FDA 510(k) clearance?

RELIANT LASER SYSTEM II received FDA 510(k) clearance on 2004-06-15, under 510(k) number K040617.

Who is the listed applicant for RELIANT LASER SYSTEM II?

The FDA 510(k) record lists Reliant Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RELIANT LASER SYSTEM II?

The FDA product code for RELIANT LASER SYSTEM II is GEX. This falls under the Gastroenterology category.

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Other records listing Reliant Technologies, 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.

K080915FRAXEL RE:PAIR (FRAXEL III SR) LASER SYSTEM AND ACCESSORIESK071051FRAXEL III SR LASER SYSTEM AND ACCESSORIESK071621RELIANT TECHNOLOGIES C300 CHILLER SYSTEM AND ACCESSORIESK070284FRALEX SR 1500 LASER SYSTEM (FRALEX II SR LASER SYSTEM)K063038FRAXEL III SR LASER SYSTEM AND ACCESSORIESK063808FRAXEL IV SR LASER SYSTEM

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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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