FDA 510(k) Applications Submitted by SHAMROCK MANUFACTURING COMPANY

FDA 510(k) Number Submission Date Device Name Applicant
K030386 02/05/2003 POWDER FREE SYNTHETIC NITRILE NEOPRENE EXAMINATION GLOVES, SIZES SMALL,MEDIUM, LARGE, AND X-LARGE SHAMROCK MANUFACTURING COMPANY
K012786 08/20/2001 POWDERFREE NITRILE NEOPRENE EXAMINATION GLOVES (PULPLE) SHAMROCK MANUFACTURING COMPANY


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