FDA device listing
Accuwell T4 Neonatal Screening EIA,BioDominium Diagnostics T4 Neonatal Screening EIA,PRIME T4 Neonatal Screening…
FDA device listing 1497926644 · ASTORIA-PACIFIC, INC.
Key facts
| Proprietary names | Accuwell T4 Neonatal Screening EIA,BioDominium Diagnostics T4 Neonatal Screening EIA,PRIME T4 Neonatal Screening EIA,SPOTCHECK T4 Neonatal Screening Kit |
|---|---|
| Owner/operator | ASTORIA-PACIFIC, INC. |
| Owner/operator number | 3050015 |
| Premarket submissions | K972974 |
| Product codes | KLI |
| Device names | KLI - Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1700 |
| Review panels | Clinical Chemistry |
| Registered establishments | ASTORIA-PACIFIC, INC. |
| Establishment registrations | 3050015 |
| FEI numbers | 3050015 |
| Establishment operations | Complaint File Establishment, 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