Data / Medical devices / United States / Jones Medical Instrument Co.
Jones Medical Instrument Co.: FDA-registered device maker in Oak Brook, IL, United States, 1 510(k) clearance
Jones Medical Instrument Co. is registered with the FDA (registration 1416588) in Oak Brook, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 20, 1981. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 1416588
- Address
- 200 Windsor Dr, Oak Brook, IL, United States, 60523
- Owner or operator
- JONES MEDICAL INSTRUMENT CO. (1416588)
- Roles
- Manufacturer
- First device listed
- March 21, 2008
- Registered through
- 2026
- Brand names listed
- Satellite
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Calculator, Pulmonary Function Data | BZC | 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 |
|---|---|---|---|---|---|---|
| August 20, 1981 | K812001 | OSCILLAIRE | BZC | Substantially Equivalent | Jones Medical Instrument Co. | accessdata.fda.gov |
Compare with other makers
Updated August 20, 1981. 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.