FDA device listing
Single-Loop Snare Retrieval Kit,Triple-Loop Snare Retieval Kit
FDA device listing 1598055237 · ARGON MEDICAL DEVICES, INC
Key facts
| Proprietary names | Single-Loop Snare Retrieval Kit,Triple-Loop Snare Retieval Kit |
|---|---|
| Owner/operator | ARGON MEDICAL DEVICES, INC |
| Owner/operator number | 9059795 |
| Premarket submissions | K191758 |
| Product codes | MMX |
| Device names | MMX - Device, Percutaneous Retrieval |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.5150 |
| Review panels | Cardiovascular |
| Registered establishments | ARGON MEDICAL DEVICES INC. |
| Establishment registrations | 1625425 |
| FEI numbers | 1625425 |
| Establishment operations | 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