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FDA 510(k), K060269, ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM
FDA 510(k), K060269, ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM
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510(K) Number: K060269
Device Name: ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM
Manufacturer: ACMI CORPORATION
Device Classification Name: Choledochoscope And Accessories, Flexible/Rigid
Regulation Number: 876.1500
Classification Product Code: FBN
Date Received: 02/01/2006
Decision Date: 03/31/2006
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM
Manufacturer: ACMI CORPORATION
Device Classification Name: Choledochoscope And Accessories, Flexible/Rigid
Regulation Number: 876.1500
Classification Product Code: FBN
Date Received: 02/01/2006
Decision Date: 03/31/2006
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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