Data / Medical devices / United States / BTI Filtration
BTI Filtration: FDA-registered device maker in Oklahoma City, OK, United States, 1 510(k) clearance
BTI Filtration is registered with the FDA (registration 1651723) in Oklahoma City, OK, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 2, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1651723
- FEI number
- 3003200197
- Address
- 4000 N Stiles Ave, Oklahoma City, OK, United States, 73105
- Owner or operator
- 4M VENTURES, INC. DBA BTI Filtration (9072105)
- Roles
- Manufacturer
- First device listed
- June 5, 2008
- Registered through
- 2026
- Brand names listed
- BTI Carbon Exchange Service, BTI Filtration Deionizer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Subsystem, Water Purification | FIP | 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 |
|---|---|---|---|---|---|---|
| June 2, 2008 | K080703 | BTI FILTRATION DEIONIZATION EXCHANGE TANK; BTI FILTRATION CARBON EXCHANGE TANK | FIP | Substantially Equivalent | 4m Ventures, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 2, 2008. 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.