FDA 510(k), K972699, AESOP 3000 SYSTEM AND ACCESSORIES

510(K) Number: K972699
Device Name: AESOP 3000 SYSTEM AND ACCESSORIES
Manufacturer: COMPUTER MOTION, INC.
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 07/18/1997
Decision Date: 12/19/1997
Regulation Medical Specialty: Gastroenterology/Urology

210 pages (280 of 490 original pages are fully redacted)