Litho 60; Litho 100; Litho 150
K-Number: K242251 · 2024-09-03
ApplicantQuanta System Spa
Decision Date2024-09-03
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Litho 60; Litho 100; Litho 150 is a medical device manufactured by Quanta System Spa. It received FDA 510(k) clearance on 2024-09-03 under approval number K242251. 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 Litho 60; Litho 100; Litho 150?
Litho 60; Litho 100; Litho 150 is a medical device that received FDA 510(k) clearance on 2024-09-03. It is manufactured by Quanta System Spa. The 510(k) number is K242251.
When was Litho 60; Litho 100; Litho 150 approved by the FDA?
Litho 60; Litho 100; Litho 150 received FDA 510(k) clearance on 2024-09-03, under approval number K242251.
What company makes Litho 60; Litho 100; Litho 150?
Litho 60; Litho 100; Litho 150 is manufactured by Quanta System Spa.
What is the FDA product code for Litho 60; Litho 100; Litho 150?
The FDA product code for Litho 60; Litho 100; Litho 150 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.