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FDA 510(k), K760822, MODEL TX-8 PANENDOSCOPE
FDA 510(k), K760822, MODEL TX-8 PANENDOSCOPE
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510(K) Number: K760822
Device Name: MODEL TX-8 PANENDOSCOPE
Manufacturer: AMERICAN CYSTOCOPE MAKERS, INC.
Device Classification Name: panendoscope (gastroduodenoscope)
Regulation Number: 876.1500
Classification Product Code: FAK
Date Received: 10/13/1976
Decision Date: 10/21/1976
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: MODEL TX-8 PANENDOSCOPE
Manufacturer: AMERICAN CYSTOCOPE MAKERS, INC.
Device Classification Name: panendoscope (gastroduodenoscope)
Regulation Number: 876.1500
Classification Product Code: FAK
Date Received: 10/13/1976
Decision Date: 10/21/1976
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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