Data / Medical devices / United States / Elixir Corporation
Elixir Corporation: FDA-registered device maker in Suwanee, GA, United States, 1 510(k) clearance
Elixir Corporation is registered with the FDA (registration 3008513006) in Suwanee, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 23, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008513006
- Address
- 305 Shawnee North Dr Ste 250, Suwanee, GA, United States, 30024
- Owner or operator
- Atlanta Biomedical Corporation (10032392)
- Roles
- Manufacturer
- First device listed
- May 10, 2010
- Registered through
- 2026
- Brand names listed
- ABC Model 4100 Infusion Pump
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pump, Infusion | FRN | 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 |
|---|---|---|---|---|---|---|
| October 23, 2008 | K072603 | ABC SYRINGE INFUSION PUMP, MODEL 4100 | FRN | Substantially Equivalent | Elixir Corporation | accessdata.fda.gov |
Compare with other makers
Updated October 23, 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.