510(k) K261315

Device
Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 Family
Applicant
Siemens Medical Solutions USA, Inc.
510(k) number
K261315
Product code
KPS
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-21
Date received
2026-04-21
Regulation
892.1200
Classification name
System, Tomography, Computed, Emission
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Tabitha Estes
Address
810 Innovation Dr. Knoxville TN US 37932 37932

FDA Registration Numbers

Source Documents

510(k) summary PDF

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