Data / Medical devices / United States / Medical Decision Network
Medical Decision Network: FDA-registered device maker in Charlottesville, VA, United States, 1 510(k) clearance
Medical Decision Network is registered with the FDA (registration 3010817588) in Charlottesville, VA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 15, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010817588
- Address
- 2220 Ivy Rd Suite 402, Charlottesville, VA, United States, 22903
- Owner or operator
- Medical Decision Network (10046643)
- Roles
- Manufacturer
- First device listed
- January 12, 2015
- Registered through
- 2026
- Brand names listed
- GlucoStabilizer, GlucoStabilizer Insulin Dosing Calculator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Calculator, Drug Dose | NDC | 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 |
|---|---|---|---|---|---|---|
| September 15, 2014 | K141321 | GLUCOSTABILIZER INSULIN DOSING CALCULATOR | NDC | Substantially Equivalent | Medical Decision Network | accessdata.fda.gov |
Compare with other makers
Updated September 15, 2014. 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.