FDA 510(k), K103429, BIOGRAPH MMR

FDA 510(k), K103429, BIOGRAPH MMR

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510(K) Number: K103429
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: 11/22/2010
Decision Date: 06/08/2011
Regulation Medical Specialty: Radiology
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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