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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name biopsy needle
510(k) Number K840354
Device Name MONOJECT SOFT TISSUE BIOPSY/FINE NEEDLE
Applicant
SHERWOOD MEDICAL CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
SHERWOOD MEDICAL CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.1075
Classification Product Code
FCG  
Date Received01/26/1984
Decision Date 03/12/1984
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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