510(k) K221680

Device
Xeleris V Processing and Review System
Applicant
GE Healthcare
510(k) number
K221680
Product code
LLZ
Decision
Substantially Equivalent (SESE)
Decision date
2023-03-01
Date received
2022-06-09
Regulation
892.2050
Classification name
System, Image Processing, Radiological
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
George Mashour
Address
4 Hayozma St. Tirat Hacarmel IL 30200 30200

FDA Registration Numbers

Source Documents

510(k) summary PDF

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