FDA device listing
Radioimmunoassay, Human Growth Hormone
FDA device listing 1905099086 · Diagnostic Automation /Cortez Diagnostics Inc.
Key facts
| Owner/operator | Diagnostic Automation /Cortez Diagnostics Inc. |
|---|---|
| Owner/operator number | 9011974 |
| Product codes | CFL |
| Device names | CFL - Radioimmunoassay, Human Growth Hormone |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.1370 |
| Review panels | Clinical Chemistry |
| Registered establishments | Diagnostic Automation/ Cortez Diagnostics Inc,. |
| Establishment registrations | 2029372 |
| FEI numbers | 1000306617 |
| 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