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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Needle, Fistula
510(k) Number K801632
Device Name THE BELLCO FISTULA NEEDLES
Applicant
Bellco Artifidial Organ Spec., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Bellco Artifidial Organ Spec., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number876.5540
Classification Product Code
FIE  
Date Received07/15/1980
Decision Date 08/04/1980
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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