LASEMD Laser System
K-Number: K171009 · 2017-06-23
ApplicantLutronic Corporation
Decision Date2017-06-23
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
LASEMD Laser System is a medical device manufactured by Lutronic Corporation. It received FDA 510(k) clearance on 2017-06-23 under approval number K171009. 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 LASEMD Laser System?
LASEMD Laser System is a medical device that received FDA 510(k) clearance on 2017-06-23. It is manufactured by Lutronic Corporation. The 510(k) number is K171009.
When was LASEMD Laser System approved by the FDA?
LASEMD Laser System received FDA 510(k) clearance on 2017-06-23, under approval number K171009.
What company makes LASEMD Laser System?
LASEMD Laser System is manufactured by Lutronic Corporation.
What is the FDA product code for LASEMD Laser System?
The FDA product code for LASEMD Laser 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.