FDA device listing
Peripheral Catheter Insertion Kit
FDA device listing 1622052593 · ARGON MEDICAL DEVICES, INC
Key facts
| Owner/operator | ARGON MEDICAL DEVICES, INC |
|---|---|
| Owner/operator number | 9059795 |
| Product codes | OWL |
| Device names | OWL - Peripheral Catheter Insertion Kit |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5200 |
| Review panels | General Hospital |
| Registered establishments | ARGON MEDICAL DEVICES INC. |
| Establishment registrations | 1625425 |
| FEI numbers | 1625425 |
| Establishment operations | Manufacturer, Repackager/Relabeler |
| 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