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FDA 510(k), K863920, WAKO(TM) ZN TEST
FDA 510(k), K863920, WAKO(TM) ZN TEST
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510(K) Number: K863920
Device Name: WAKO(TM) ZN TEST
Manufacturer: WAKO CHEMICALS, USA, INC.
Device Classification Name:
Regulation Number:
Classification Product Code:
Date Received: 10/08/1986
Decision Date: 09/16/1987
Regulation Medical Specialty:
Device Name: WAKO(TM) ZN TEST
Manufacturer: WAKO CHEMICALS, USA, INC.
Device Classification Name:
Regulation Number:
Classification Product Code:
Date Received: 10/08/1986
Decision Date: 09/16/1987
Regulation Medical Specialty:
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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. Learn more about Fast-Track Requests here.
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