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FDA 510(k), K904931, AUTO SUTURE(R) PERMANENT PURSTRING(TM) APPLIER*
FDA 510(k), K904931, AUTO SUTURE(R) PERMANENT PURSTRING(TM) APPLIER*
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510(K) Number: K904931
Device Name: AUTO SUTURE(R) PERMANENT PURSTRING(TM) APPLIER*
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: suture, nonabsorbable, synthetic, polyamide
Regulation Number: 878.5020
Classification Product Code: GAR
Date Received: 10/31/1990
Decision Date: 01/29/1991
Regulation Medical Specialty: General & Plastic Surgery
Device Name: AUTO SUTURE(R) PERMANENT PURSTRING(TM) APPLIER*
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: suture, nonabsorbable, synthetic, polyamide
Regulation Number: 878.5020
Classification Product Code: GAR
Date Received: 10/31/1990
Decision Date: 01/29/1991
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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