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FDA 510(k), K133226, BIOGRAPH MMR
FDA 510(k), K133226, BIOGRAPH MMR
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510(K) Number: K133226
Device Name: BIOGRAPH MMR
Manufacturer: SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Classification Name: tomographic imager combining emission computed tomography with nuclear magnetic resonance
Regulation Number: 892.1200
Classification Product Code: OUO
Date Received: 10/21/2013
Decision Date: 11/12/2013
Regulation Medical Specialty: Radiology
Device Name: BIOGRAPH MMR
Manufacturer: SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Classification Name: tomographic imager combining emission computed tomography with nuclear magnetic resonance
Regulation Number: 892.1200
Classification Product Code: OUO
Date Received: 10/21/2013
Decision Date: 11/12/2013
Regulation Medical Specialty: Radiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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