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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 K844551
Device Name HOBBS MEDICAL /JAYCO MULTIPLE BIOPSY INSTRUMENT
Applicant
GOBBS MEDICAL, INC.
497 N. MAIN ST.
PALMER,  MA  01069
Applicant Contact STEVEN G RICHTER
Correspondent
GOBBS MEDICAL, INC.
497 N. MAIN ST.
PALMER,  MA  01069
Correspondent Contact STEVEN G RICHTER
Regulation Number876.1075
Classification Product Code
FCL  
Date Received11/21/1984
Decision Date 01/03/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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