FDA device listing
FREND PSA
FDA device listing 1717427491 · Alius Scientific, LLC
Key facts
| Proprietary names | FREND PSA |
|---|---|
| Owner/operator | Alius Scientific, LLC |
| Owner/operator number | 10072559 |
| Premarket submissions | K124056 |
| Product codes | KHO, LTJ |
| Device names | KHO - Fluorometer, For Clinical Use, LTJ - Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers |
| Device class | Class I, Class II |
| Classification regulations (21 CFR) | 862.2560, 866.6010 |
| Review panels | Clinical Chemistry, Immunology |
| Registered establishments | Alius Scientific,LLC |
| Establishment registrations | 3010324880 |
| FEI numbers | 3010324880 |
| Establishment operations | Complaint File Establishment |
| 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