Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Laparoscope, General & Plastic Surgery
510(k) Number K931783
Device Name AESOP (AUTOMATED ENDOSCOPIC SYSTEM FOR OPTIMAL POS
Applicant
COMPUTER MOTION, INC.
700 THIRTEENTH ST. N.W.
SUITE 1200
WASHINGTON,  DC  20005
Applicant Contact THOMAS SCARLETT
Correspondent
COMPUTER MOTION, INC.
700 THIRTEENTH ST. N.W.
SUITE 1200
WASHINGTON,  DC  20005
Correspondent Contact THOMAS SCARLETT
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received04/09/1993
Decision Date 11/22/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-