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
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
- 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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