FDA device listing
Fecal Occult Blood (FOB) Rapid Test Kit (Immunochromatographic Assay)
FDA device listing 1281672231 · BioTeke Corporation (Wuxi) Co., Ltd
Key facts
| Proprietary names | Fecal Occult Blood (FOB) Rapid Test Kit (Immunochromatographic Assay) |
|---|---|
| Owner/operator | BioTeke Corporation (Wuxi) Co., Ltd |
| Owner/operator number | 10071745 |
| Product codes | OSL |
| Device names | OSL - Control, Fecal Occult Blood |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.6550 |
| Review panels | Hematology |
| Registered establishments | BIOTEKE CORPORATION (WUXI) CO., LTD |
| Establishment registrations | 3016837106 |
| FEI numbers | 3016837106 |
| Establishment operations | Manufacturer |
| 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