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FDA 510(k), K163141, NAMIC ClearaCIL Contrast Injection Lines
FDA 510(k), K163141, NAMIC ClearaCIL Contrast Injection Lines
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$149.00 USD
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510(K) Number: K163141
Device Name: NAMIC ClearaCIL Contrast Injection Lines
Manufacturer: AngioDynamics, Inc.
Device Classification Name: catheter, intravascular, diagnostic
Regulation Number: 870.1200
Classification Product Code: DQO
Date Received: 11/09/2016
Decision Date: 01/06/2017
Regulation Medical Specialty: Cardiovascular
Device Name: NAMIC ClearaCIL Contrast Injection Lines
Manufacturer: AngioDynamics, Inc.
Device Classification Name: catheter, intravascular, diagnostic
Regulation Number: 870.1200
Classification Product Code: DQO
Date Received: 11/09/2016
Decision Date: 01/06/2017
Regulation Medical Specialty: Cardiovascular
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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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