FDA device listing
ID NOW COVID-19 2.0,ID NOW COVID-19 2.0 Control Swab Kit
FDA device listing 1719541611 · ABBOTT LABORATORIES
Key facts
| Proprietary names | ID NOW COVID-19 2.0,ID NOW COVID-19 2.0 Control Swab Kit |
|---|---|
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| Premarket submissions | K221925 |
| Product codes | QWR |
| Device names | QWR - Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets From Clinical Specimens In Near-Patient Settings |
| Device class | Class II |
| Classification regulations (21 CFR) | 866.3982 |
| Review panels | Microbiology |
| Registered establishments | Abbott Diagnostics Scarborough, Inc. |
| Establishment registrations | 1221359 |
| FEI numbers | 1221359 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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