FDA device listing
AutoDELFIA instrument (models 1297-014, 1297-0110, 1235-0110, 1235-5110, 1235-5220),Victor D (1420-020, 1420-021)
FDA device listing 2005253277 · Revvity, Inc.
Key facts
| Proprietary names | AutoDELFIA instrument (models 1297-014, 1297-0110, 1235-0110, 1235-5110, 1235-5220),Victor D (1420-020, 1420-021) |
|---|---|
| Owner/operator | Revvity, Inc. |
| Owner/operator number | 9912035 |
| Product codes | KHO |
| Device names | KHO - Fluorometer, For Clinical Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2560 |
| Review panels | Clinical Chemistry |
| Registered establishments | WALLAC OY |
| Establishment registrations | 8043909 |
| FEI numbers | 3002808498 |
| Establishment operations | Complaint File Establishment, 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