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FDA 510(k), K091869, SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS
FDA 510(k), K091869, SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS
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510(K) Number: K091869
Device Name: SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS
Manufacturer: COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
Device Classification Name: laparoscope, general & plastic surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 06/23/2009
Decision Date: 09/01/2009
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS
Manufacturer: COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
Device Classification Name: laparoscope, general & plastic surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 06/23/2009
Decision Date: 09/01/2009
Regulation Medical Specialty: Gastroenterology/Urology
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