FDA device listing
ARK™ EDDP Assay,ARK™ EDDP Calibrator,ARK™ EDDP Control
FDA device listing 1684484016 · ARK Diagnostics Inc
Key facts
| Proprietary names | ARK™ EDDP Assay,ARK™ EDDP Calibrator,ARK™ EDDP Control |
|---|---|
| Owner/operator | ARK Diagnostics Inc |
| Owner/operator number | 10027663 |
| Premarket submissions | K182779 |
| Product codes | DJR |
| Device names | DJR - Enzyme Immunoassay, Methadone |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.3620 |
| Review panels | Clinical Toxicology |
| Registered establishments | ARK DIAGNOSTICS INC |
| Establishment registrations | 3005755244 |
| FEI numbers | 3005755244 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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