Data / Medical devices / United States / Alco Sales & Service Co.
Alco Sales & Service Co.: FDA-registered device maker in Burr Ridge, IL, United States, 1 510(k) clearance
Alco Sales & Service Co. is registered with the FDA (registration 1423561) in Burr Ridge, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 12, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1423561
- FEI number
- 3000210114
- Address
- 6851 High Grove BLVD, Burr Ridge, IL, United States, 60527
- Owner or operator
- ALCO Sales and Service Co (10051003)
- Roles
- Specification developer
- First device listed
- January 25, 2016
- Registered through
- 2026
- Brand names listed
- ALCO CLASSIC
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Mechanical | IOR | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| March 12, 2008 | K080207 | DANYANG HUAYI K2 AND K7 WHEELCHAIRS | IOR | Substantially Equivalent | Danyang Huayi Medical Supply & Equipment Co, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 12, 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.