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FDA 510(k), K111825, ENDO GIA(TM) STAPLERS, DST SERIES(TM) GIA(TM) STAPLERS, DST SERIES(TM) TA(TM) STAPLERS
FDA 510(k), K111825, ENDO GIA(TM) STAPLERS, DST SERIES(TM) GIA(TM) STAPLERS, DST SERIES(TM) TA(TM) STAPLERS
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510(K) Number: K111825
Device Name: ENDO GIA(TM) STAPLERS, DST SERIES(TM) GIA(TM) STAPLERS, DST SERIES(TM) TA(TM) STAPLERS
Manufacturer: COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H
Device Classification Name: staple, implantable
Regulation Number: 878.4750
Classification Product Code: GDW
Date Received: 06/28/2011
Decision Date: 10/25/2011
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ENDO GIA(TM) STAPLERS, DST SERIES(TM) GIA(TM) STAPLERS, DST SERIES(TM) TA(TM) STAPLERS
Manufacturer: COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H
Device Classification Name: staple, implantable
Regulation Number: 878.4750
Classification Product Code: GDW
Date Received: 06/28/2011
Decision Date: 10/25/2011
Regulation Medical Specialty: General & Plastic Surgery
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- Delivery: Approximately 1 to 2 weeks
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