FDA device listing
OnSite hCG Combo Rapid Test (REF# R1001C),OnSite hCG Combo Rapid Test (REF# R1001S),OnSite hCG Urine Rapid Test (REF#…
FDA device listing 1425545228 · CTK BIOTECH, INC.
Key facts
| Proprietary names | OnSite hCG Combo Rapid Test (REF# R1001C),OnSite hCG Combo Rapid Test (REF# R1001S),OnSite hCG Urine Rapid Test (REF# R1000C),OnSite hCG Urine Rapid Test (REF# R1000S) |
|---|---|
| Owner/operator | CTK BIOTECH, INC. |
| Owner/operator number | 9051784 |
| Product codes | JHI |
| Device names | JHI - Visual, Pregnancy Hcg, Prescription Use |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1155 |
| Review panels | Clinical Chemistry |
| Registered establishments | CTK BIOTECH, INC. |
| Establishment registrations | 2032682 |
| FEI numbers | 3003952975 |
| 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