FDA 510(k), K901040, IONOMETER EH-F AND ACCESSORIES
FDA 510(k), K901040, IONOMETER EH-F AND ACCESSORIES
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510(K) Number: K901040
Device Name: IONOMETER EH-F AND ACCESSORIES
Manufacturer: FRESENIUS USA, INC.
Device Classification Name: Electrode, Ion Specific, Sodium
Regulation Number: 862.1665
Classification Product Code: JGS
Date Received: 03/06/1990
Decision Date: 07/19/1990
Regulation Medical Specialty: Clinical Chemistry
Device Name: IONOMETER EH-F AND ACCESSORIES
Manufacturer: FRESENIUS USA, INC.
Device Classification Name: Electrode, Ion Specific, Sodium
Regulation Number: 862.1665
Classification Product Code: JGS
Date Received: 03/06/1990
Decision Date: 07/19/1990
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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