FDA device listing
Multi-Analyte Controls Unassayed
FDA device listing 1802461686 · MEDTOX DIAGNOSTICS, INC.
Key facts
| Owner/operator | MEDTOX DIAGNOSTICS, INC. |
|---|---|
| Owner/operator number | 1050155 |
| Product codes | OHQ |
| Device names | OHQ - Multi-Analyte Controls Unassayed |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.1660 |
| Review panels | Clinical Chemistry |
| Registered establishments | MEDTOX DIAGNOSTICS, INC. |
| Establishment registrations | 1050155, 3004175381 |
| FEI numbers | 1050155, 3004175381 |
| Establishment operations | Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database