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FDA 510(k), K922123, AUTO SUTURE DISPOSABLE ENDOSCOPIC SPECIMEN POUCH
FDA 510(k), K922123, AUTO SUTURE DISPOSABLE ENDOSCOPIC SPECIMEN POUCH
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510(K) Number: K922123
Device Name: AUTO SUTURE DISPOSABLE ENDOSCOPIC SPECIMEN POUCH
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: laryngoscope, endoscope
Regulation Number: 876.1500
Classification Product Code: GCI
Date Received: 05/06/1992
Decision Date: 02/01/1993
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: AUTO SUTURE DISPOSABLE ENDOSCOPIC SPECIMEN POUCH
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: laryngoscope, endoscope
Regulation Number: 876.1500
Classification Product Code: GCI
Date Received: 05/06/1992
Decision Date: 02/01/1993
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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