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FDA 510(k), K161723, ulrich Transfer Set
FDA 510(k), K161723, ulrich Transfer Set
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$149.00 USD
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$149.00 USD
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510(K) Number: K161723
Device Name: ulrich Transfer Set
Manufacturer: ulrich GmbH & Co. KG
Device Classification Name: iodinated contrast media transfer tubing set
Regulation Number: 880.5440
Classification Product Code: PQH
Date Received: 06/22/2016
Decision Date: 12/21/2016
Regulation Medical Specialty: General Hospital
Device Name: ulrich Transfer Set
Manufacturer: ulrich GmbH & Co. KG
Device Classification Name: iodinated contrast media transfer tubing set
Regulation Number: 880.5440
Classification Product Code: PQH
Date Received: 06/22/2016
Decision Date: 12/21/2016
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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