510(k) K251671

Biograph Vision PET/CT Systems; Biograph mCT PET/CT Systems by Siemens Medical Solutions USA, Inc. — Product Code KPS

K251671 is an FDA 510(k) premarket notification submitted by Siemens Medical Solutions USA, Inc. for the device "Biograph Vision PET/CT Systems; Biograph mCT PET/CT Systems". The FDA issued a decision of Substantially Equivalent on July 3, 2025. The device falls under product code KPS (System, Tomography, Computed, Emission), a Class II device regulated under 21 CFR 892.1200. Siemens Medical Solutions USA, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 3, 2025
Date Received
May 30, 2025
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Tomography, Computed, Emission
Device Class
Class II
Regulation Number
892.1200
Review Panel
RA
Submission Type