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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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