FDA Registration
Active
🇺🇸 United States
EPIQ 5 Ultrasound System
Reg #: 3019216
·
FEI: 3019216
·
Expires 2025
Products
3
Proprietary Names
23
Establishment Types
1
Classifications
3
Registration Details
- Registration Name
- Philips Ultrasound LLC
- Registration Number
- 3019216
- FEI Number
- 3019216
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- Yes
- Address
- 22100 Bothell Everett Hwy
- City
- BOTHELL
- State
- WA
- ZIP
- 98021
- Country
- US
Regulatory Submissions
- 510(k) Number
- K212777
Owner / Operator
- Firm Name
- Philips Medical Systems International BV
- Operator Number
- 1217116
- Address
- Veenpluis 6
- City
- Best
- State
- NL-NOTA
- Postal Code
- 5684PC
- Country
- NL
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | Class 2 | Radiology | No | 2021-09-27 |
| System, Image Processing, Radiological | LLZ | Class 2 | Radiology | No | 2021-09-27 |
| System, Imaging, Pulsed Doppler, Ultrasonic | IYN | Class 2 | Radiology | No | 2021-09-27 |
Proprietary Names
EPIQ 5 Ultrasound System
Affiniti 30 Ultrasound System
Affiniti 30 Diamond Select Ultrasound System
EPIQ CVxi Ultrasound System
Affiniti 70 Diamond Select Ultrasound System
EPIQ CVx Ultrasound System
Affiniti 70 Ultrasound System
EPIQ 5 Diamond Select Ultrasound System
EPIQ Elite Diagnostic Ultrasound System
EPIQ 7 Ultrasound System
EPIQ CVx Circular Edition Ultrasound System
Affiniti 50 Circular Edition Ultrasound System
Affiniti 50 Diamond Select Ultrasound System
EPIQ 7 Diamond Select Ultrasound System
Affiniti 50 Ultrasound System
Affiniti CVx Ultrasound System
EPIQ 5W Ultrasound System
EPIQ 7W Ultrasound System
EPIQ Elite Circular Edition Ultrasound System
Affiniti 30 Circular Edition Ultrasound System
Affiniti 70 Circular Edition Ultrasound System
EPIQ 5 Circular Edition Ultrasound System
EPIQ 7 Circular Edition Ultrasound System
Establishment Types
Manufacture Medical Device