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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instrument, Manual, Specialized Obstetric-Gynecologic
510(k) Number K810483
Device Name FALLOPIAN TUBE FORCEPS
Applicant
AMERICAN V. MUELLER
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
AMERICAN V. MUELLER
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number884.4530
Classification Product Code
KNA  
Date Received02/23/1981
Decision Date 03/11/1981
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
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