DeviceClearance

ViroZap Indoor Air Purifier, In Duct Model 1008— 510(k) K241140

Substantially Equivalent

Applied Photonix, LLC

FDA 510(k) clearance K241140 for ViroZap Indoor Air Purifier, In Duct Model 1008, Substantially Equivalent on 2024-08-01. Applicant: Applied Photonix, LLC.

Clearance details

Applicant
Applied Photonix, LLC
Product code
Code FRA
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Tampa, FL, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.