ViroZap Indoor Air Purifier, In Duct Model 1008
K-Number: K241140 · 2024-08-01
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.