510(k) K133226
K133226 is an FDA 510(k) premarket notification submitted by Siemens Medical Solutions USA, Inc. for the device "BIOGRAPH MMR". The FDA issued a decision of Substantially Equivalent on Nov 12, 2013. 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 784 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 12, 2013
- Date Received
- Oct 21, 2013
- Clearance Type
- Special
- 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
- 510(k)
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.