Class Class II

ViroZap Indoor Air Purifier, In Duct Model 1008 (K241140)

K241140 2024-08-01 Traditional
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Description

ViroZap Indoor Air Purifier, In Duct Model 1008 by Applied Photonix, LLC — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241140
Clearance Date2024-08-01
Clearance TypeTraditional
Product CodeFRA
Regulation Number880.6500

Categories

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