ViroZap Indoor Air Purifier, In Duct Model 1008— 510(k) K241140
Substantially EquivalentApplied 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. Device class: 2.
Clearance details
- Applicant
- Applied Photonix, LLC
- Product code
- Code FRA
- Device class
- Class 2
- Regulation
- 21 CFR 880.6500
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tampa, FL, US
Recent devices under product code FRA
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