Data / Medical devices / United States / Evoqua Water Technologies - South Windsor
Evoqua Water Technologies - South Windsor: FDA-registered device maker in South Windsor, CT, United States, 1 510(k) clearance
Evoqua Water Technologies - South Windsor is registered with the FDA (registration 3006029151) in South Windsor, CT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 22, 2000. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006029151
- Address
- 88 Nutmeg Road, South Windsor, CT, United States, 06074
- Owner or operator
- Evoqua Water Technologies, LLC (10057016)
- Roles
- Manufacturer
- First device listed
- February 9, 2018
- Registered through
- 2026
- Brand names listed
- SDI Exchange Tanks
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 |
|---|---|---|---|---|---|---|
| December 22, 2000 | K994279 | PURE WATER-CDS (CENTRAL DIALYSIS SOLUTION) | FIP | Substantially Equivalent | Pure Water Solutions, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 22, 2000. 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.