510(k) K260087

Device
Senographe Pristina; SenoBright HD; Pristina Serena; Pristina Serena Bright
Applicant
GE Medical Systems SCS
510(k) number
K260087
Product code
MUE
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-24
Date received
2026-01-12
Regulation
892.1715
Classification name
Full Field Digital, System, X-Ray, Mammographic
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Fayçal Kherra
Address
283, Rue De La Miniere Buc FR 78530 78530

FDA Registration Numbers

Source Documents

510(k) summary PDF

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