FDA Registration Active 🇺🇸 United States

Affiniti 30 Diamond Select Ultrasound System

Reg #: 3017894900 · FEI: 3017894900 · Expires 2025
Products
5
Proprietary Names
23
Establishment Types
1
Classifications
5

Registration Details

Registration Name
Philips Ultrasound LLC
Registration Number
3017894900
FEI Number
3017894900
Status
Active
Expiry Year
2025
Initial Importer
No
Address
222 Jacobs Street
City
Cambridge
State
MA
ZIP
02141
Country
US

Regulatory Submissions

510(k) Number
K212704

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

Proprietary Names

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

Establishment Types

Develop Specifications But Do Not Manufacture At This Facility