MEDIYAG
K-Number: K231948 · 2024-10-09
ApplicantMedicreations, LLC
Decision Date2024-10-09
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
MEDIYAG is a medical device manufactured by Medicreations, LLC. It received FDA 510(k) clearance on 2024-10-09 under approval number K231948. 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 MEDIYAG?
MEDIYAG is a medical device that received FDA 510(k) clearance on 2024-10-09. It is manufactured by Medicreations, LLC. The 510(k) number is K231948.
When was MEDIYAG approved by the FDA?
MEDIYAG received FDA 510(k) clearance on 2024-10-09, under approval number K231948.
What company makes MEDIYAG?
MEDIYAG is manufactured by Medicreations, LLC.
What is the FDA product code for MEDIYAG?
The FDA product code for MEDIYAG 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.