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FDA 510(k)

ViroZap Indoor Air Purifier, In Duct Model 1008

K-Number: K241140 · 2024-08-01

Decision Date2024-08-01
Product CodeFRA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Applied Photonix, LLC. The 510(k) number is K241140.

When was ViroZap Indoor Air Purifier, In Duct Model 1008 approved by the FDA?

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

What company makes ViroZap Indoor Air Purifier, In Duct Model 1008?

ViroZap Indoor Air Purifier, In Duct Model 1008 is manufactured by Applied Photonix, LLC.

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.

Related Devices (Code: FRA)

Official Source

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