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FDA 510(k), K901107, MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC
FDA 510(k), K901107, MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC
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510(K) Number: K901107
Device Name: MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: clamp, surgical, general & plastic surgery
Regulation Number: 878.4800
Classification Product Code: GDJ
Date Received: 03/08/1990
Decision Date: 04/09/1990
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: clamp, surgical, general & plastic surgery
Regulation Number: 878.4800
Classification Product Code: GDJ
Date Received: 03/08/1990
Decision Date: 04/09/1990
Regulation Medical Specialty: General & Plastic Surgery
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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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