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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Collector, Urine, (And Accessories) For Indwelling Catheter
510(k) Number K802737
Device Name URINE COLLECTION BAG TYPE 1590V
Applicant
BIO D CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BIO D CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number876.5250
Classification Product Code
KNX  
Date Received11/03/1980
Decision Date 12/18/1980
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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