510(k) K172531
K172531 is an FDA 510(k) premarket notification submitted by Siemens Medical Solutions USA, Inc. for the device "Biograph mMR with mMR Angio Transfer Option". The FDA issued a decision of Substantially Equivalent on November 14, 2017. The device falls under product code OUO (Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance), 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
- November 14, 2017
- Date Received
- August 22, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance
- Device Class
- Class II
- Regulation Number
- 892.1200
- Review Panel
- RA
- Submission Type
Imager that generates both both magnetic resonance (mr) and positron emission tomography (pet) images and provides registration and fusion of these images. Pet and mr images can be acquired either simultaneously or sequentially. Anatomical mr images are used for pet attenuation correction.