FDA 510(k), K935071, INSULATED FORCEPS, BIOPSY FORCEPS, SCISSORS

FDA 510(k), K935071, INSULATED FORCEPS, BIOPSY FORCEPS, SCISSORS

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510(K) Number: K935071
Device Name: INSULATED FORCEPS, BIOPSY FORCEPS, SCISSORS
Manufacturer: KARL STORZ ENDOSCOPY-AMERICA, INC.
Device Classification Name: laparoscope, general & plastic surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 10/25/1993
Decision Date: 04/25/1994
Regulation Medical Specialty: Gastroenterology/Urology

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