StarWalker
K-Number: K171227 · 2017-08-18
ApplicantFotona D.O.O.
Decision Date2017-08-18
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
StarWalker is a medical device manufactured by Fotona D.O.O.. It received FDA 510(k) clearance on 2017-08-18 under approval number K171227. 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 StarWalker?
StarWalker is a medical device that received FDA 510(k) clearance on 2017-08-18. It is manufactured by Fotona D.O.O.. The 510(k) number is K171227.
When was StarWalker approved by the FDA?
StarWalker received FDA 510(k) clearance on 2017-08-18, under approval number K171227.
What company makes StarWalker?
StarWalker is manufactured by Fotona D.O.O..
What is the FDA product code for StarWalker?
The FDA product code for StarWalker 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.