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FDA 510(k), K172394, Steerable Guide Catheter
FDA 510(k), K172394, Steerable Guide Catheter
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510(K) Number: K172394
Device Name: Steerable Guide Catheter
Manufacturer: Abbott Vascular
Device Classification Name: catheter, steerable
Regulation Number: 870.1280
Classification Product Code: DRA
Date Received: 08/08/2017
Decision Date: 09/06/2017
Regulation Medical Specialty: Cardiovascular
Device Name: Steerable Guide Catheter
Manufacturer: Abbott Vascular
Device Classification Name: catheter, steerable
Regulation Number: 870.1280
Classification Product Code: DRA
Date Received: 08/08/2017
Decision Date: 09/06/2017
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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