FDA device listing
CareSuperb COVID-19 Antigen External Control,CareSuperb COVID-19 Antigen Home Test,CareSuperb COVID-19 Antigen Test
FDA device listing 2055607328 · Access Bio, Inc.
Key facts
| Proprietary names | CareSuperb COVID-19 Antigen External Control,CareSuperb COVID-19 Antigen Home Test,CareSuperb COVID-19 Antigen Test |
|---|---|
| Owner/operator | Access Bio, Inc. |
| Owner/operator number | 10028116 |
| Premarket submissions | K241915 |
| Product codes | QYT |
| Device names | QYT - Over-The-Counter Covid-19 Antigen Test |
| Device class | Class II |
| Classification regulations (21 CFR) | 866.3984 |
| Review panels | Microbiology |
| Registered establishments | Access Bio, Inc. |
| Establishment registrations | 3024756665 |
| FEI numbers | 3024756665 |
| Establishment operations | Manufacturer |
| 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