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FDA 510(k), K943997, BEHRING NEPHELOMETER II
FDA 510(k), K943997, BEHRING NEPHELOMETER II
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510(K) Number: K943997
Device Name: BEHRING NEPHELOMETER II
Manufacturer: BEHRING DIAGNOSTICS, INC.
Device Classification Name: igg, antigen, antiserum, control
Regulation Number: 866.5510
Classification Product Code: DEW
Date Received: 08/16/1994
Decision Date: 10/03/1994
Regulation Medical Specialty: Immunology
Device Name: BEHRING NEPHELOMETER II
Manufacturer: BEHRING DIAGNOSTICS, INC.
Device Classification Name: igg, antigen, antiserum, control
Regulation Number: 866.5510
Classification Product Code: DEW
Date Received: 08/16/1994
Decision Date: 10/03/1994
Regulation Medical Specialty: Immunology
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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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