FDA Registration Active 🇺🇸 United States

EPIQ Series Diagnostic Ultrasound System

Reg #: 2518586 · FEI: 2518586 · Expires 2025
Products
5
Proprietary Names
25
Establishment Types
1
Classifications
5

Registration Details

Registration Name
Philips Ultrasound LLC
Registration Number
2518586
FEI Number
2518586
Status
Active
Expiry Year
2025
Initial Importer
No
Address
1 Echo Dr
City
Reedsville
State
PA
ZIP
17084
Country
US

Regulatory Submissions

510(k) Number
K211597

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
Transducer, Ultrasonic, Diagnostic ITX
System, Imaging, Pulsed Echo, Ultrasonic IYO
Automated Radiological Image Processing Software QIH
Catheter, Ultrasound, Intravascular OBJ
System, Imaging, Pulsed Doppler, Ultrasonic IYN

Proprietary Names

EPIQ Series Diagnostic Ultrasound System Affiniti 30 Ultrasound System Affiniti 70 Diamond Select Ultrasound System EPIQ Elite Diagnostic Ultrasound System Affiniti 30 Diamond Select Ultrasound System EPIQ 5W Ultrasound System Affiniti CVx Ultrasound System EPIQ 7 Ultrasound System Affiniti Series Diagnostic Ultrasound System Affiniti 50 Diamond Select Ultrasound System EPIQ CVx Ultrasound System EPIQ 5 Diamond Select Ultrasound System EPIQ 7W Ultrasound System EPIQ CVxi Ultrasound System EPIQ 7 Diamond Select Ultrasound System Affiniti 50 Ultrasound System EPIQ 5 Ultrasound System Affiniti 70 Ultrasound System Affiniti 70 Circular Edition Ultrasound System EPIQ CVx Circular Edition Ultrasound System EPIQ Elite Circular Edition Ultrasound System EPIQ 5 Circular Edition Ultrasound System Affiniti 50 Circular Edition Ultrasound System EPIQ 7 Circular Edition Ultrasound System Affiniti 30 Circular Edition Ultrasound System

Establishment Types

Manufacture Medical Device