FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

Senographe Pristina; SenoBright HD; Pristina Serena; Pristina Serena Bright

K Number: K260087 · Decision Mar 24, 2026
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
54
Applicant Total
37
Review Days
71

Basic Information

Device Name
Senographe Pristina; SenoBright HD; Pristina Serena; Pristina Serena Bright
K Number
K260087
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1715
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Medical Systems SCS
Date Received
January 12, 2026
Decision Date
March 24, 2026
Product Code
MUE
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MUE Full Field Digital, System, X-Ray, Mammographic

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