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FDA 510(k), K132535, AUTOBAND LIGATOR
FDA 510(k), K132535, AUTOBAND LIGATOR
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510(K) Number: K132535
Device Name: AUTOBAND LIGATOR
Manufacturer: ENDOCHOICE, INC.
Device Classification Name: ligator, esophageal
Regulation Number: 876.4400
Classification Product Code: MND
Date Received: 08/13/2013
Decision Date: 08/23/2013
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: AUTOBAND LIGATOR
Manufacturer: ENDOCHOICE, INC.
Device Classification Name: ligator, esophageal
Regulation Number: 876.4400
Classification Product Code: MND
Date Received: 08/13/2013
Decision Date: 08/23/2013
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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