FDA device listing
Radifocus Glidewire Advantage 0.014
FDA device listing 1570278470 · TERUMO CORP.
Key facts
| Proprietary names | Radifocus Glidewire Advantage 0.014 |
|---|---|
| Owner/operator | TERUMO CORP. |
| Owner/operator number | 8010026 |
| Premarket submissions | K122590 |
| Product codes | DQX |
| Device names | DQX - Wire, Guide, Catheter |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1330 |
| Review panels | Cardiovascular |
| Registered establishments | ASHITAKA FACTORY OF TERUMO CORP., TERUMO CORP., Terumo Yamaguchi Corporation |
| Establishment registrations | 8010026, 9681834, 3013611763 |
| FEI numbers | 2828, 3002808327, 3013611763 |
| Establishment operations | Contract Manufacturer, Contract Sterilizer, Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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