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FDA 510(k), K851058, DOSI FLOW
FDA 510(k), K851058, DOSI FLOW
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510(K) Number: K851058
Device Name: DOSI FLOW
Manufacturer: JUAN ALFONSO
Device Classification Name: Controller, Infusion, Intravascular, Electronic
Regulation Number: LDR
Classification Product Code: 03/14/1985
Date Received: 04/29/1985
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: DOSI FLOW
Manufacturer: JUAN ALFONSO
Device Classification Name: Controller, Infusion, Intravascular, Electronic
Regulation Number: LDR
Classification Product Code: 03/14/1985
Date Received: 04/29/1985
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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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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