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FDA 510(k), K062850, AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS
FDA 510(k), K062850, AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS
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510(K) Number: K062850
Device Name: AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: staple, implantable
Regulation Number: 878.4750
Classification Product Code: GDW
Date Received: 09/25/2006
Decision Date: 10/23/2006
Regulation Medical Specialty: General & Plastic Surgery
Device Name: AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS
Manufacturer: UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Device Classification Name: staple, implantable
Regulation Number: 878.4750
Classification Product Code: GDW
Date Received: 09/25/2006
Decision Date: 10/23/2006
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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