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FDA 510(k), K060258, AUTOFUSER
FDA 510(k), K060258, AUTOFUSER
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510(K) Number: K060258
Device Name: AUTOFUSER
Manufacturer: ACE MEDICAL US, LLC
Device Classification Name: pump, infusion, elastomeric
Regulation Number: 880.5725
Classification Product Code: MEB
Date Received: 02/01/2006
Decision Date: 05/30/2006
Regulation Medical Specialty: General Hospital
Device Name: AUTOFUSER
Manufacturer: ACE MEDICAL US, LLC
Device Classification Name: pump, infusion, elastomeric
Regulation Number: 880.5725
Classification Product Code: MEB
Date Received: 02/01/2006
Decision Date: 05/30/2006
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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