Data / Medical devices / United States / Applied Photonix LLC
Applied Photonix LLC: FDA-registered device maker in Tampa, FL, United States, 1 510(k) clearance
Applied Photonix LLC is registered with the FDA (registration 3032191707) in Tampa, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 1, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3032191707
- Address
- 3802 Spectrum Blvd suite 202, Tampa, FL, United States, 33612
- Owner or operator
- Applied Photonix LLC (10091316)
- Roles
- Manufacturer
- First device listed
- August 21, 2024
- Registered through
- 2026
- Brand names listed
- ViroZap
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Purifier, Air, Ultraviolet, Medical | FRA | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 1, 2024 | K241140 | ViroZap Indoor Air Purifier, In Duct Model 1008 | FRA | Substantially Equivalent | Applied Photonix, LLC | accessdata.fda.gov |
Compare with other makers
Updated August 1, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.