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FDA 510(k), K925689, MERIDIAN EBV-IGG TEST KIT
FDA 510(k), K925689, MERIDIAN EBV-IGG TEST KIT
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510(K) Number: K925689
Device Name: MERIDIAN EBV-IGG TEST KIT
Manufacturer: FULLER LABORATORIES, INC.
Device Classification Name: antigen, ebv, capsid
Regulation Number: 866.3235
Classification Product Code: MCD
Date Received: 11/12/1992
Decision Date: 10/12/1993
Regulation Medical Specialty: Microbiology
Device Name: MERIDIAN EBV-IGG TEST KIT
Manufacturer: FULLER LABORATORIES, INC.
Device Classification Name: antigen, ebv, capsid
Regulation Number: 866.3235
Classification Product Code: MCD
Date Received: 11/12/1992
Decision Date: 10/12/1993
Regulation Medical Specialty: Microbiology
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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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