Data / Medical devices / United States / General Medical Co.
General Medical Co.: FDA-registered device maker in Jacksonville, FL, United States, 1 510(k) clearance
General Medical Co. is registered with the FDA (registration 3013399500) in Jacksonville, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 19, 1983. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013399500
- Address
- 5011 Gate Parkway, Bldg. 100 Suite 100, Jacksonville, FL, United States, 32256
- Owner or operator
- GENERAL MEDICAL CO. (2012353)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- December 14, 2015
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Iontophoresis, Other Uses | EGJ | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| July 19, 1983 | K831320 | DRIONIC | EGJ | Substantially Equivalent | General Medical Co. | accessdata.fda.gov |
Compare with other makers
Updated July 19, 1983. 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.