FDA 510(k), K100593, SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME
FDA 510(k), K100593, SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME
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510(K) Number: K100593
Device Name: SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME
Manufacturer: LSI SOLUTIONS, INC.
Device Classification Name: suture, nonabsorbable, synthetic, polypropylene
Regulation Number: 878.5010
Classification Product Code: GAW
Date Received: 03/02/2010
Decision Date: 10/13/2010
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME
Manufacturer: LSI SOLUTIONS, INC.
Device Classification Name: suture, nonabsorbable, synthetic, polypropylene
Regulation Number: 878.5010
Classification Product Code: GAW
Date Received: 03/02/2010
Decision Date: 10/13/2010
Regulation Medical Specialty: General & Plastic Surgery
- 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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