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FDA 510(k), K091773, FUJINON STERILE OVERTUBES
FDA 510(k), K091773, FUJINON STERILE OVERTUBES
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$149.00 USD
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510(K) Number: K091773
Device Name: FUJINON STERILE OVERTUBES
Manufacturer: FUJINON, INC.
Device Classification Name: endoscopic access overtube, gastroenterology-urology
Regulation Number: 876.1500
Classification Product Code: FED
Date Received: 06/16/2009
Decision Date: 08/07/2009
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: FUJINON STERILE OVERTUBES
Manufacturer: FUJINON, INC.
Device Classification Name: endoscopic access overtube, gastroenterology-urology
Regulation Number: 876.1500
Classification Product Code: FED
Date Received: 06/16/2009
Decision Date: 08/07/2009
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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