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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Forceps, Biopsy, Gynecological
510(k) Number K802458
Device Name KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611
Applicant
J. Sklar Mfg. Co., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
J. Sklar Mfg. Co., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number884.4530
Classification Product Code
HFB  
Date Received10/08/1980
Decision Date 01/12/1981
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
Recalls CDRH Recalls
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