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FDA 510(k), K141117, EZ-IO INTRAOSSEOUS INFUSION SYSTEM
FDA 510(k), K141117, EZ-IO INTRAOSSEOUS INFUSION SYSTEM
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510(K) Number: K141117
Device Name: EZ-IO INTRAOSSEOUS INFUSION SYSTEM
Manufacturer: VIDACARE LLC
Device Classification Name: needle, hypodermic, single lumen
Regulation Number: 880.5570
Classification Product Code: FMI
Date Received: 04/30/2014
Decision Date: 07/08/2014
Regulation Medical Specialty: General Hospital
Device Name: EZ-IO INTRAOSSEOUS INFUSION SYSTEM
Manufacturer: VIDACARE LLC
Device Classification Name: needle, hypodermic, single lumen
Regulation Number: 880.5570
Classification Product Code: FMI
Date Received: 04/30/2014
Decision Date: 07/08/2014
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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