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FDA 510(k), K130468, ORBIT INFUSION SET
FDA 510(k), K130468, ORBIT INFUSION SET
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510(K) Number: K130468
Device Name: ORBIT INFUSION SET
Manufacturer: YPSOMED AG
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 02/25/2013
Decision Date: 03/19/2013
Regulation Medical Specialty: General Hospital
Device Name: ORBIT INFUSION SET
Manufacturer: YPSOMED AG
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 02/25/2013
Decision Date: 03/19/2013
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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