Data / Medical devices / United States / Electrochemical Oxygen Concepts
Electrochemical Oxygen Concepts: FDA-registered device maker in San Antonio, TX, United States, 1 510(k) clearance
Electrochemical Oxygen Concepts is registered with the FDA (registration 3008139322) in San Antonio, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 12, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008139322
- FEI number
- 3009589269
- Address
- 12500 Network Blvd Ste 310, San Antonio, TX, United States, 78249
- Owner or operator
- Electrochemical Oxygen Concepts dba EO2 Concepts (10030899)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- November 25, 2009
- Registered through
- 2026
- Brand names listed
- Carrying Case, Dual Port Cannula, 36", Extension Set, 72", Humidicant Pack, OxyGeni Power Pack, OxyGeni Starter Kit, OxySpur Lite Oxygen Diffusion Dressing, 2x8, Adhesive, OxySpur Oxygen Diffusion Dressing, 2x2, Adhesive and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chamber, Oxygen, Topical, Extremity | KPJ | 2 | Complaint file establishment, 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 12, 2009 | K090681 | TANSCU O2 | KPJ | Substantially Equivalent | Electrochemical Oxygen Concepts, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 12, 2009. 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.