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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, Non-Electric
510(k) Number K871710
Device Name BIOPSY FORCEPS
Applicant
Frantz Medical Development, Ltd.
595 Madison Ave.
New York,  NY  10022
Applicant Contact MARK G FRANTZ
Correspondent
Frantz Medical Development, Ltd.
595 Madison Ave.
New York,  NY  10022
Correspondent Contact MARK G FRANTZ
Regulation Number876.1075
Classification Product Code
FCL  
Date Received05/01/1987
Decision Date 08/10/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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