FDA device listing
Coagulation Factor Deficient Plasma
FDA device listing 2030384003 · GEORGE KING BIO-MEDICAL, INC.
Key facts
| Proprietary names | Coagulation Factor Deficient Plasma |
|---|---|
| Owner/operator | GEORGE KING BIO-MEDICAL, INC. |
| Owner/operator number | 1928890 |
| Product codes | GJT |
| Device names | GJT - Plasma, Coagulation Factor Deficient |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.7290 |
| Review panels | Hematology |
| Registered establishments | GEORGE KING BIO-MEDICAL, INC. |
| Establishment registrations | 1928890 |
| FEI numbers | 1928890 |
| 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