FDA device listing
Venclose digiRF Generator,Venclose EVSRF Catheter,Venclose Foot Pedal,Venclose Power Cord,Venclose RF Ablation…
FDA device listing 1600976819 · C. R. Bard, Inc.
Key facts
| Proprietary names | Venclose digiRF Generator,Venclose EVSRF Catheter,Venclose Foot Pedal,Venclose Power Cord,Venclose RF Ablation Catheter,Venclose System |
|---|---|
| Owner/operator | C. R. Bard, Inc. |
| Owner/operator number | 2212754 |
| Premarket submissions | K160754 |
| Product codes | GEI |
| Device names | GEI - Electrosurgical, Cutting & Coagulation & Accessories |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4400 |
| Review panels | General & Plastic Surgery |
| Registered establishments | BARD PERIPHERAL VASCULAR, INC. |
| Establishment registrations | 2020394 |
| FEI numbers | 2020394 |
| Establishment operations | Complaint File Establishment |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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