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FDA 510(k)

VasQ

K-Nummer: K240119 · 2024-02-16

AntragstellerLaminate Medical Technologies , Ltd.
Entscheidungsdatum2024-02-16
ProduktcodeQVQ
BeratungsausschussCV
EntscheidungSubstantially Equivalent

Produktübersicht

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.

Häufig gestellte Fragen

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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