FDA 510(k)

Qlicksmart BladeFlask UNIVERSAL

N.º K: K213274 · 2022-06-22

Fecha de decisión2022-06-22

Código de productoMMK

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Qlicksmart BladeFlask UNIVERSAL is the device name listed in this FDA 510(k) record. The listed applicant is Qlicksmart Pty , Ltd.. It received FDA 510(k) clearance on 2022-06-22 under 510(k) number K213274. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Qlicksmart BladeFlask UNIVERSAL?

Qlicksmart BladeFlask UNIVERSAL is a medical device that received FDA 510(k) clearance on 2022-06-22. The listed applicant is Qlicksmart Pty , Ltd.. The 510(k) number is K213274.

When did Qlicksmart BladeFlask UNIVERSAL receive FDA 510(k) clearance?

Qlicksmart BladeFlask UNIVERSAL received FDA 510(k) clearance on 2022-06-22, under 510(k) number K213274.

Who is the listed applicant for Qlicksmart BladeFlask UNIVERSAL?

The FDA 510(k) record lists Qlicksmart Pty , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Qlicksmart BladeFlask UNIVERSAL?

The FDA product code for Qlicksmart BladeFlask UNIVERSAL is MMK.

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Dispositivos relacionados (Código: MMK)

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