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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name laparoscope, general & plastic surgery
510(k) Number K991444
Device Name HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY).
Applicant
COMPUTER MOTION, INC.
130-B CREMONA DR.
GOLETA,  CA  93117
Applicant Contact DAVID THOMAS
Correspondent
COMPUTER MOTION, INC.
130-B CREMONA DR.
GOLETA,  CA  93117
Correspondent Contact DAVID THOMAS
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received04/26/1999
Decision Date 06/25/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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