FDA device listing
Serum Diluent IgM, Conjugate IgM, Conjugate IgA
FDA device listing 1934094959 · SAVYON DIAGNOSTICS, LTD.
Key facts
| Proprietary names | Serum Diluent IgM, Conjugate IgM, Conjugate IgA |
|---|---|
| Owner/operator | SAVYON DIAGNOSTICS, LTD. |
| Owner/operator number | 8030129 |
| Product codes | PPM |
| Device names | PPM - General Purpose Reagent |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.4010 |
| Review panels | Pathology |
| Registered establishments | SAVYON DIAGNOSTICS LTD. |
| Establishment registrations | 8030124 |
| FEI numbers | 3003206361 |
| 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