DIODE LASER THERAPY SYSTEMS
K-Number: K152898 · 2016-02-09
Decision Date2016-02-09
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
DIODE LASER THERAPY SYSTEMS is a medical device manufactured by Beijing Sincoheren Science and Tech. Development Co., Ltd.. It received FDA 510(k) clearance on 2016-02-09 under approval number K152898. 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 DIODE LASER THERAPY SYSTEMS?
DIODE LASER THERAPY SYSTEMS is a medical device that received FDA 510(k) clearance on 2016-02-09. It is manufactured by Beijing Sincoheren Science and Tech. Development Co., Ltd.. The 510(k) number is K152898.
When was DIODE LASER THERAPY SYSTEMS approved by the FDA?
DIODE LASER THERAPY SYSTEMS received FDA 510(k) clearance on 2016-02-09, under approval number K152898.
What company makes DIODE LASER THERAPY SYSTEMS?
DIODE LASER THERAPY SYSTEMS is manufactured by Beijing Sincoheren Science and Tech. Development Co., Ltd..
What is the FDA product code for DIODE LASER THERAPY SYSTEMS?
The FDA product code for DIODE LASER THERAPY SYSTEMS is GEX. This falls under the Gastroenterology category.
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Official Source
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