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FDA 510(k), K133987, CAPTIVATOR II,SINGLE-USE POLYPECTOMY SNARES
FDA 510(k), K133987, CAPTIVATOR II,SINGLE-USE POLYPECTOMY SNARES
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510(K) Number: K133987
Device Name: CAPTIVATOR II,SINGLE-USE POLYPECTOMY SNARES
Manufacturer: Boston Scientific Corporation
Device Classification Name: snare, flexible
Regulation Number: 876.4300
Classification Product Code: FDI
Date Received: 12/26/2013
Decision Date: 01/24/2014
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: CAPTIVATOR II,SINGLE-USE POLYPECTOMY SNARES
Manufacturer: Boston Scientific Corporation
Device Classification Name: snare, flexible
Regulation Number: 876.4300
Classification Product Code: FDI
Date Received: 12/26/2013
Decision Date: 01/24/2014
Regulation Medical Specialty: Gastroenterology/Urology
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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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