FDA device listing
SARS-CoV-2 IgM & IgG Test System
FDA device listing 1786335703 · TECO DIAGNOSTICS
Key facts
| Proprietary names | SARS-CoV-2 IgM & IgG Test System |
|---|---|
| Owner/operator | TECO DIAGNOSTICS |
| Owner/operator number | 1832216 |
| Product codes | QKO |
| Device names | QKO - Reagent, Coronavirus Serological |
| Device class | Not classified |
| Classification regulations (21 CFR) | ORCA1.QKO |
| Review panels | Microbiology |
| Registered establishments | TECO DIAGNOSTICS |
| Establishment registrations | 1832216 |
| FEI numbers | 1832216 |
| Establishment operations | U.S. Manufacturer of Export Only Devices |
| 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