FDA device listing
Non-Sterile Cable (Controller to Pump or Remote Control)
FDA device listing 1236137615 · Amphenol DC Electronics
Key facts
| Proprietary names | Non-Sterile Cable (Controller to Pump or Remote Control) |
|---|---|
| Owner/operator | Amphenol DC Electronics |
| Owner/operator number | 10043592 |
| Product codes | LPB |
| Device names | LPB - Cardiac Ablation Percutaneous Catheter |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.LPB |
| Review panels | Cardiovascular |
| Registered establishments | AMPHENOL DC ELECTRONICS |
| Establishment registrations | 3001763079 |
| FEI numbers | 3001763079 |
| Establishment operations | Contract Manufacturer |
| 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