FDA device listing
Advisor FL Mapping Catheter, Sensor Enabled Software Installation, H702507,Advisor HD Grid Mapping Catheter, Sensor…
FDA device listing 2059853676 · ABBOTT LABORATORIES
Key facts
| Proprietary names | Advisor FL Mapping Catheter, Sensor Enabled Software Installation, H702507,Advisor HD Grid Mapping Catheter, Sensor Enbled Software Installation, H702519,Advisor HD/VL Mapping Catheter, Catheter Catalog Installation Sensor Enabled, H702532,AutoMark Installation Kit, H702499-HW,AutoMark Software Installation v.1.0, H702499,Ensite™ Amplifier and Display Workstation, EE3000,EnSite™ ArrayLink™ Module… |
|---|---|
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| Premarket submissions | K201181 |
| Product codes | DQK |
| Device names | DQK - Computer, Diagnostic, Programmable |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1425 |
| Review panels | Cardiovascular |
| Registered establishments | Abbott Medical Costa Rica Ltda., IRVINE BIOMEDICAL. INC., St. Jude Medical, St. Jude Medical, Atrial Fibrillation Division, Inc., St. Jude Medical, Cardiology Division, Inc. |
| Establishment registrations | 2030404, 2184149, 3005334138, 3008452825, 3012179728 |
| FEI numbers | 1000139754, 1000519796, 3005334138, 3008452825, 3012179728 |
| Establishment operations | Complaint File Establishment, Manufacturer, Specification Developer |
| 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