Data / Medical devices / United States / Applied Neuroscience, Inc.
Applied Neuroscience, Inc.: FDA-registered device maker in Redington Shores, FL, United States, 1 510(k) clearance
Applied Neuroscience, Inc. is registered with the FDA (registration 3004577596) in Redington Shores, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 3, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004577596
- Address
- 248 176TH Terrace DR E, Redington Shores, FL, United States, 33708
- Owner or operator
- APPLIED NEUROSCIENCE, INC. (9063417)
- Roles
- Manufacturer
- First device listed
- November 12, 2007
- Registered through
- 2026
- Brand names listed
- Neuroguide
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Normalizing Quantitative Electroencephalograph Software | OLU | 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 3, 2004 | K041263 | NEUROGUIDE ANALYSIS SYSTEM | OLU | Substantially Equivalent | Applied Neuroscience, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 3, 2004. 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.