Data / Medical devices / United States / Magstim Inc
Magstim Inc: FDA-registered device maker in Eugene, OR, United States, 2 510(k) clearances
Magstim Inc is registered with the FDA (registration 3017666517) in Eugene, OR, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 12, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017666517
- FEI number
- 3001090553
- Address
- 78 Centennial Loop Suite C, Eugene, OR, United States, 97401
- Owner or operator
- The Magstim Company Ltd. (8021774)
- Roles
- Manufacturer
- First device listed
- September 4, 2020
- Registered through
- 2026
- Brand names listed
- GES 400,GES 405, GES 410, Geosource 2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Full-Montage Standard Electroencephalograph | GWQ | 2 | Manufacturer | accessdata.fda.gov |
| Non-Normalizing Quantitative Electroencephalograph Software | OLT | 2 | Manufacturer | accessdata.fda.gov |
| Source Localization Software For Electroencephalograph Or Magnetoencephalograph | OLX | 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 12, 2014 | K131882 | GEODESICEEG SYSTEM 400 SERIES (GES 400) | OLT | Substantially Equivalent | Electrical Geodesics, Inc. | accessdata.fda.gov |
| December 21, 2010 | K092844 | GEOSOURCE | OLX | Substantially Equivalent | Electrical Geodesics, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Non-Normalizing Quantitative Electroencephalograph Software
- All makers of Full-Montage Standard Electroencephalograph
- All makers of Source Localization Software For Electroencephalograph Or Magnetoencephalograph
Updated February 12, 2014. 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.