FDA device listing
VCP RHEUMATOID FACTOR CALIBRATOR KIT 16
FDA device listing 1226315947 · DENKA CO., LTD.
Key facts
| Proprietary names | VCP RHEUMATOID FACTOR CALIBRATOR KIT 16 |
|---|---|
| Owner/operator | DENKA CO., LTD. |
| Owner/operator number | 9053049 |
| Product codes | DHR |
| Device names | DHR - System, Test, Rheumatoid Factor |
| Device class | Class II |
| Classification regulations (21 CFR) | 866.5775 |
| Review panels | Immunology |
| Registered establishments | DENKA CO., LTD. |
| Establishment registrations | 3003871639 |
| FEI numbers | 3003871639 |
| Establishment operations | Contract 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