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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Curette, Suction, Endometrial (And Accessories)
510(k) Number K823080
Device Name VAKUTAGE
Applicant
WESTON, COPCO, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
WESTON, COPCO, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number884.1175
Classification Product Code
HHK  
Date Received10/19/1982
Decision Date 11/24/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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