CorNeat EverPatch
K-Number: K223074 · 2023-06-02
ApplicantCorneat Vision , Ltd.
Decision Date2023-06-02
Product CodeQWU
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
CorNeat EverPatch is the device name listed in this FDA 510(k) record. The listed applicant is Corneat Vision , Ltd.. It received FDA 510(k) clearance on 2023-06-02 under 510(k) number K223074. The device is classified under product code QWU. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CorNeat EverPatch?
CorNeat EverPatch is a medical device that received FDA 510(k) clearance on 2023-06-02. The listed applicant is Corneat Vision , Ltd.. The 510(k) number is K223074.
When did CorNeat EverPatch receive FDA 510(k) clearance?
CorNeat EverPatch received FDA 510(k) clearance on 2023-06-02, under 510(k) number K223074.
Who is the listed applicant for CorNeat EverPatch?
The FDA 510(k) record lists Corneat Vision , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CorNeat EverPatch?
The FDA product code for CorNeat EverPatch is QWU.
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.