510(k) K241140

Device
ViroZap Indoor Air Purifier, In Duct Model 1008
Applicant
Applied Photonix, LLC
510(k) number
K241140
Product code
FRA
Decision
Substantially Equivalent (SESE)
Decision date
2024-08-01
Date received
2024-04-24
Regulation
880.6500
Classification name
Purifier, Air, Ultraviolet, Medical
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
D. Yogi Goswami
Address
3802 Spectrum Blvd. Suite 202-1 Tampa FL US 33612 33612

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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