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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name system, abortion, vacuum
510(k) Number K900641
Device Name CANNULA, SUCTION UTERINE
Applicant
WILLIAMS SPECIALTY PRODUCTS, INC.
3700 WESTFALL DR.
ENCINO,  CA  91436
Applicant Contact WILLIAMS, MD
Correspondent
WILLIAMS SPECIALTY PRODUCTS, INC.
3700 WESTFALL DR.
ENCINO,  CA  91436
Correspondent Contact WILLIAMS, MD
Regulation Number884.5070
Classification Product Code
HHI  
Date Received02/09/1990
Decision Date 03/30/1990
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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