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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name brush, scrub, operating-room
510(k) Number K831226
Device Name MEDICAL PRODUCTS FOAM DOUBLE SCRUB #450
Applicant
BALLARD MEDICAL PRODUCTS
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BALLARD MEDICAL PRODUCTS
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4800
Classification Product Code
GEC  
Date Received04/15/1983
Decision Date 05/16/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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