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FDA 510(k)

VISUALASE THERMAL THERAPY SYSTEM

K-Number: K071328 · 2007-08-31

ApplicantBiotex, Inc.
Decision Date2007-08-31
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VISUALASE THERMAL THERAPY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biotex, Inc.. It received FDA 510(k) clearance on 2007-08-31 under 510(k) number K071328. 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 VISUALASE THERMAL THERAPY SYSTEM?

VISUALASE THERMAL THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 2007-08-31. The listed applicant is Biotex, Inc.. The 510(k) number is K071328.

When did VISUALASE THERMAL THERAPY SYSTEM receive FDA 510(k) clearance?

VISUALASE THERMAL THERAPY SYSTEM received FDA 510(k) clearance on 2007-08-31, under 510(k) number K071328.

Who is the listed applicant for VISUALASE THERMAL THERAPY SYSTEM?

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

What is the FDA product code for VISUALASE THERMAL THERAPY SYSTEM?

The FDA product code for VISUALASE THERMAL THERAPY SYSTEM is GEX. This falls under the Gastroenterology category.

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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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