FDA 510(k), K820723, KODAK EKTACHEM CLINICAL CHEM. NH3
FDA 510(k), K820723, KODAK EKTACHEM CLINICAL CHEM. NH3
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510(K) Number: K820723
Device Name: KODAK EKTACHEM CLINICAL CHEM. NH3
Manufacturer: EASTMAN KODAK COMPANY
Device Classification Name: Photometric Method, Ammonia
Regulation Number: 862.1065
Classification Product Code: JID
Date Received: 03/16/1982
Decision Date: 04/01/1982
Regulation Medical Specialty: Clinical Chemistry
Device Name: KODAK EKTACHEM CLINICAL CHEM. NH3
Manufacturer: EASTMAN KODAK COMPANY
Device Classification Name: Photometric Method, Ammonia
Regulation Number: 862.1065
Classification Product Code: JID
Date Received: 03/16/1982
Decision Date: 04/01/1982
Regulation Medical Specialty: Clinical Chemistry
- 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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