K241140
- 510(k) number
- K241140
- Device name
- ViroZap Indoor Air Purifier, In Duct Model 1008
- Applicant
- Applied Photonix, LLC FL · US
- Product code
- FRA — Purifier, Air, Ultraviolet, Medical
- Decision date
- 2024-08-01
- Date received
- 2024-04-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
510(k) Summary (official FDA PDF): K241140.pdf
Official FDA record: K241140
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.