FDA device listing
8 CHANNEL FOOT ANKLE COIL 1.5T,8 Channel Foot Ankle MR Coil Kit 1.5T,8 Channel Foot Ankle MR Coil Kit 3.0T,8CH FOOT…
FDA device listing 1913997375 · Philips Medical Systems International BV
Key facts
| Proprietary names | 8 CHANNEL FOOT ANKLE COIL 1.5T,8 Channel Foot Ankle MR Coil Kit 1.5T,8 Channel Foot Ankle MR Coil Kit 3.0T,8CH FOOT ANKLE MR COIL 3T,dS FOOTANKLE 8CH 1.5T,dS FootAnkle 8Ch 3.0T,dS Foot-Ankle Coil 8ch 3.0T,GE Excite 1.5T 8Ch Foot and Ankle Coil (FAC),GE Excite 3.0T HDx 8Ch FAC,GE Excite HDx 1.5T HDx 8Ch 1.5T FAC,GE HD 1.5T 8C Foot and Ankle,GE HD 3.0T 8C Foot and Ankle,HD 8Ch Foot Ankle Coil,HD 8CH… |
|---|---|
| Owner/operator | Philips Medical Systems International BV |
| Owner/operator number | 1217116 |
| Premarket submissions | K050514 |
| Product codes | MOS |
| Device names | MOS - Coil, Magnetic Resonance, Specialty |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.1000 |
| Review panels | Radiology |
| Registered establishments | Philips Electronics Ltd, Philips Global Business Services LLP, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Establishment registrations | 3000126629, 3016851825, 3042177665 |
| FEI numbers | 3000126629, 3016851825, 3042177665 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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