510(k) K211215

Device
SenoBright HD
Applicant
GE Healthcare
510(k) number
K211215
Product code
MUE
Decision
Substantially Equivalent (SESE)
Decision date
2021-06-22
Date received
2021-04-23
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
No

Related Records

Applicant Contact

Contact
Florian Akpakpa
Address
283 Rue De La Minière Buc FR 78530 78530

FDA Registration Numbers

Source Documents

510(k) summary PDF

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