FDA device listing
5000 Compact Series Ultrasound Systems,Deluxe Compact Cart,Extended Compact Cart,Premium Compact Cart,Ultrasound System…
FDA device listing 1729933378 · Philips Medical Systems International BV
Key facts
| Proprietary names | 5000 Compact Series Ultrasound Systems,Deluxe Compact Cart,Extended Compact Cart,Premium Compact Cart,Ultrasound System 5300G,Ultrasound System 5300P,Ultrasound System 5300W,Ultrasound System 5500CV,Ultrasound System 5500G,Ultrasound System 5500P,Ultrasound System 5500W |
|---|---|
| Owner/operator | Philips Medical Systems International BV |
| Owner/operator number | 1217116 |
| Premarket submissions | K222648 |
| Product codes | ITX, IYN, IYO |
| Device names | ITX - Transducer, Ultrasonic, Diagnostic, IYN - System, Imaging, Pulsed Doppler, Ultrasonic, IYO - System, Imaging, Pulsed Echo, Ultrasonic |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.1550, 892.1560, 892.1570 |
| Review panels | Radiology |
| Registered establishments | Philips Electronics Ltd, Philips Ultrasound LLC |
| Establishment registrations | 3019216, 3000126629, 3017894900 |
| FEI numbers | 3019216, 3000126629, 3017894900 |
| Establishment operations | Complaint File Establishment, Manufacturer, Foreign Exporter, Specification Developer |
| 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