FDA device listing
5F Super Torque MB Diagnostic Catheter
FDA device listing 1258595950 · Cordis US Corp.
Key facts
| Proprietary names | 5F Super Torque MB Diagnostic Catheter |
|---|---|
| Owner/operator | Cordis US Corp. |
| Owner/operator number | 1016427 |
| Premarket submissions | K212977 |
| Product codes | DQO |
| Device names | DQO - Catheter, Intravascular, Diagnostic |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1200 |
| Review panels | Cardiovascular |
| Registered establishments | Cardinal Health Mexico 244 S de RL de CV, Cordis US Corp. |
| Establishment registrations | 1016427, 9616099 |
| FEI numbers | 1016427, 3003528016 |
| Establishment operations | Complaint File Establishment, Specification Developer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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