VasQ
Номер K: K240119 · 2024-02-16
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ЗаявительLaminate Medical Technologies , Ltd.
Дата решения2024-02-16
Код продуктаQVQ
Консультативный комитетCV
РешениеSubstantially Equivalent
Описание устройства
VasQ is the device name listed in this FDA 510(k) record. The listed applicant is Laminate Medical Technologies , Ltd.. It received FDA 510(k) clearance on 2024-02-16 under 510(k) number K240119. The device is classified under product code QVQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Часто задаваемые вопросы
What is the VasQ?
VasQ is a medical device that received FDA 510(k) clearance on 2024-02-16. The listed applicant is Laminate Medical Technologies , Ltd.. The 510(k) number is K240119.
When did VasQ receive FDA 510(k) clearance?
VasQ received FDA 510(k) clearance on 2024-02-16, under 510(k) number K240119.
Who is the listed applicant for VasQ?
The FDA 510(k) record lists Laminate Medical Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VasQ?
The FDA product code for VasQ is QVQ.
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