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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Curette, Uterine
510(k) Number K881794
Device Name IVORY FINDER SET
Applicant
Ivory Instruments Co.
2447 W. 250th St.
Lomita,  CA  90717
Applicant Contact EDWARD WALKER
Correspondent
Ivory Instruments Co.
2447 W. 250th St.
Lomita,  CA  90717
Correspondent Contact EDWARD WALKER
Regulation Number884.4530
Classification Product Code
HCY  
Date Received04/26/1988
Decision Date 07/08/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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