FDA device listing
Nova Allegro System
FDA device listing 2021723997 · NOVA BIOMEDICAL CORP.
Key facts
| Proprietary names | Nova Allegro System |
|---|---|
| Owner/operator | NOVA BIOMEDICAL CORP. |
| Owner/operator number | 1219029 |
| Product codes | JIR |
| Device names | JIR - Indicator Method, Protein Or Albumin (Urinary, Non-Quant.) |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.1645 |
| Review panels | Clinical Chemistry |
| Registered establishments | NOVA BIOMEDICAL CORPORATION |
| Establishment registrations | 1219029 |
| FEI numbers | 1219029 |
| Establishment operations | U.S. Manufacturer of Export Only Devices |
| 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