FDA device listing
MitraClip™ and TriClip™ Accessories – Lift,MitraClip™ and TriClip™ Accessories – Plate,MitraClip™ and TriClip™…
FDA device listing 1930101732 · ABBOTT LABORATORIES
Key facts
| Proprietary names | MitraClip™ and TriClip™ Accessories – Lift,MitraClip™ and TriClip™ Accessories – Plate,MitraClip™ and TriClip™ Accessories – Stabilizer |
|---|---|
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| Product codes | QWA |
| Device names | QWA - Cardiovascular Delivery Catheter System Positioning And Stabilization Device |
| Device class | Class I |
| Classification regulations (21 CFR) | 870.3955 |
| Review panels | Cardiovascular |
| Registered establishments | Abbott Medical, Abbott Vascular, ABBOTT VASCULAR, Abbott Vascular Netherlands |
| Establishment registrations | 2135147, 2939561, 3004091615, 3005070406, 3007113487 |
| FEI numbers | 3004091615, 3004635528, 3005070406, 3005334138, 3007113487 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Manufacturer, Specification Developer |
| 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