FRAXEL SR LASER SYSTEM
K-Number: K050841 · 2005-07-05
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Device Summary
Frequently Asked Questions
What is the FRAXEL SR LASER SYSTEM?
FRAXEL SR LASER SYSTEM is a medical device that received FDA 510(k) clearance on 2005-07-05. The listed applicant is Reliant Technologies, Inc.. The 510(k) number is K050841.
When did FRAXEL SR LASER SYSTEM receive FDA 510(k) clearance?
FRAXEL SR LASER SYSTEM received FDA 510(k) clearance on 2005-07-05, under 510(k) number K050841.
Who is the listed applicant for FRAXEL SR LASER SYSTEM?
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 FRAXEL SR LASER SYSTEM?
The FDA product code for FRAXEL SR 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 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.
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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