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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 K013069
Device Name BIOSPEED
Applicant
H.S. HOSPITAL SERVICES S.P.A.
10147 UMBERLAND PLACE
BOCA RATON,  FL  33428
Applicant Contact LUCIO IMPROTA
Correspondent
H.S. HOSPITAL SERVICES S.P.A.
10147 UMBERLAND PLACE
BOCA RATON,  FL  33428
Correspondent Contact LUCIO IMPROTA
Regulation Number876.1075
Classification Product Code
FCG  
Date Received09/13/2001
Decision Date 12/12/2001
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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