FDA 510(k)

ViroZap Indoor Air Purifier, In Duct Model 1008

N.º K: K241140 · 2024-08-01

Fecha de decisión2024-08-01

Código de productoFRA

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

ViroZap Indoor Air Purifier, In Duct Model 1008 is the device name listed in this FDA 510(k) record. The listed applicant is Applied Photonix, LLC. It received FDA 510(k) clearance on 2024-08-01 under 510(k) number K241140. The device is classified under product code FRA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ViroZap Indoor Air Purifier, In Duct Model 1008?

ViroZap Indoor Air Purifier, In Duct Model 1008 is a medical device that received FDA 510(k) clearance on 2024-08-01. The listed applicant is Applied Photonix, LLC. The 510(k) number is K241140.

When did ViroZap Indoor Air Purifier, In Duct Model 1008 receive FDA 510(k) clearance?

ViroZap Indoor Air Purifier, In Duct Model 1008 received FDA 510(k) clearance on 2024-08-01, under 510(k) number K241140.

Who is the listed applicant for ViroZap Indoor Air Purifier, In Duct Model 1008?

The FDA 510(k) record lists Applied Photonix, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ViroZap Indoor Air Purifier, In Duct Model 1008?

The FDA product code for ViroZap Indoor Air Purifier, In Duct Model 1008 is FRA.

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Fuente oficial

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