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FDA 510(k), K060479, MODIFICATION TO BODYGUARD INFUSION PUMP SYSTEM
FDA 510(k), K060479, MODIFICATION TO BODYGUARD INFUSION PUMP SYSTEM
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510(K) Number: K060479
Device Name: MODIFICATION TO BODYGUARD INFUSION PUMP SYSTEM
Manufacturer: CAESAREA MEDICAL ELECTRONICS LTD.
Device Classification Name: pump, infusion
Regulation Number: 880.5725
Classification Product Code: FRN
Date Received: 02/23/2006
Decision Date: 05/12/2006
Regulation Medical Specialty: General Hospital
Device Name: MODIFICATION TO BODYGUARD INFUSION PUMP SYSTEM
Manufacturer: CAESAREA MEDICAL ELECTRONICS LTD.
Device Classification Name: pump, infusion
Regulation Number: 880.5725
Classification Product Code: FRN
Date Received: 02/23/2006
Decision Date: 05/12/2006
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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