Data / Medical devices / United States / Airocide Systems
Airocide Systems: FDA-registered device maker in Neptune Beach, FL, United States, 1 510(k) clearance
Airocide Systems is registered with the FDA (registration 3009522781) in Neptune Beach, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 24, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009522781
- Address
- 2300 Marshpoint Road Suite 202, Neptune Beach, FL, United States, 32266
- Owner or operator
- Airocide Systems (10094867)
- Roles
- Manufacturer
- First device listed
- December 30, 2025
- Registered through
- 2026
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 |
|---|---|---|---|---|---|---|
| February 24, 2006 | K052732 | ABRACAIR AIR CLEANER, MODEL QTZ300-60; ABRACAIR AIR CLEANER, MODEL TI 100-30P | FRA | Substantially Equivalent | Abracair, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 24, 2006. 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.