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FDA 510(k), K903207, AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE
FDA 510(k), K903207, AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE
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510(K) Number: K903207
Device Name: AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: laparoscope, gynecologic (and accessories)
Regulation Number: 884.1720
Classification Product Code: HET
Date Received: 07/20/1990
Decision Date: 09/25/1990
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: laparoscope, gynecologic (and accessories)
Regulation Number: 884.1720
Classification Product Code: HET
Date Received: 07/20/1990
Decision Date: 09/25/1990
Regulation Medical Specialty: Obstetrics/Gynecology
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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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