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FDA 510(k), K110586, ADVIA CENTAUR VITAMIN D TOTAL ASSAY
FDA 510(k), K110586, ADVIA CENTAUR VITAMIN D TOTAL ASSAY
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510(K) Number: K110586
Device Name: ADVIA CENTAUR VITAMIN D TOTAL ASSAY
Manufacturer: Siemens Healthcare Diagnostics Inc.
Device Classification Name: system, test, vitamin d
Regulation Number: 862.1825
Classification Product Code: MRG
Date Received: 03/01/2011
Decision Date: 10/14/2011
Regulation Medical Specialty: Clinical Chemistry
Device Name: ADVIA CENTAUR VITAMIN D TOTAL ASSAY
Manufacturer: Siemens Healthcare Diagnostics Inc.
Device Classification Name: system, test, vitamin d
Regulation Number: 862.1825
Classification Product Code: MRG
Date Received: 03/01/2011
Decision Date: 10/14/2011
Regulation Medical Specialty: Clinical Chemistry
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- 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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