FDA 510(k), K050456, MEDRAD AVANTA FLUID MANAGEMENT INJECTION SYSTEM
FDA 510(k), K050456, MEDRAD AVANTA FLUID MANAGEMENT INJECTION SYSTEM
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510(K) Number: K050456
Device Name: MEDRAD AVANTA FLUID MANAGEMENT INJECTION SYSTEM
Manufacturer: MEDRAD, INC.
Device Classification Name: injector and syringe, angiographic
Regulation Number: 870.1650
Classification Product Code: DXT
Date Received: 02/23/2005
Decision Date: 06/17/2005
Regulation Medical Specialty: Cardiovascular
Device Name: MEDRAD AVANTA FLUID MANAGEMENT INJECTION SYSTEM
Manufacturer: MEDRAD, INC.
Device Classification Name: injector and syringe, angiographic
Regulation Number: 870.1650
Classification Product Code: DXT
Date Received: 02/23/2005
Decision Date: 06/17/2005
Regulation Medical Specialty: Cardiovascular
- 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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