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FDA 510(k), K090993, INTUITIVE SURGICAL ENDOSCOPIC INSTRUMENT CONTROL SYSTEMS, MODELS IS1200, IS2000 AND IS3000
FDA 510(k), K090993, INTUITIVE SURGICAL ENDOSCOPIC INSTRUMENT CONTROL SYSTEMS, MODELS IS1200, IS2000 AND IS3000
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510(K) Number: K090993
Device Name: INTUITIVE SURGICAL ENDOSCOPIC INSTRUMENT CONTROL SYSTEMS, MODELS IS1200, IS2000 AND IS3000
Manufacturer: INTUITIVE SURGICAL, INC.
Device Classification Name: system, surgical, computer controlled instrument
Regulation Number: 876.1500
Classification Product Code: NAY
Date Received: 04/07/2009
Decision Date: 12/16/2009
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: INTUITIVE SURGICAL ENDOSCOPIC INSTRUMENT CONTROL SYSTEMS, MODELS IS1200, IS2000 AND IS3000
Manufacturer: INTUITIVE SURGICAL, INC.
Device Classification Name: system, surgical, computer controlled instrument
Regulation Number: 876.1500
Classification Product Code: NAY
Date Received: 04/07/2009
Decision Date: 12/16/2009
Regulation Medical Specialty: Gastroenterology/Urology
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- Delivery: Approximately 1 to 2 weeks
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