FDA device listing
Maestro Foot Switch
FDA device listing 2065930430 · LINEMASTER SWITCH CORP.
Key facts
| Proprietary names | Maestro Foot Switch |
|---|---|
| Owner/operator | LINEMASTER SWITCH CORP. |
| Owner/operator number | 9080742 |
| Product codes | LPB, OAD |
| Device names | LPB - Cardiac Ablation Percutaneous Catheter, OAD - Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.LPB, ORCA1.OAD |
| Review panels | Cardiovascular |
| Registered establishments | LINEMASTER SWITCH CORP. |
| Establishment registrations | 3001592626 |
| FEI numbers | 3001592626 |
| 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