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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 K870560
Device Name COSMEDTECH CANNULA
Applicant
COSMEDTECH, INC.
5633 VIA SALEROSA
TUCSON,  AZ  85715
Applicant Contact JOHN M JOHNSON
Correspondent
COSMEDTECH, INC.
5633 VIA SALEROSA
TUCSON,  AZ  85715
Correspondent Contact JOHN M JOHNSON
Regulation Number884.5070
Classification Product Code
HHI  
Date Received02/10/1987
Decision Date 03/04/1987
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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