FDA 510(k) Applications Submitted by PT. SHAMROCK MANUFACTURING CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K030134 01/14/2003 LATEX EXAMINATION GLOVES POWDER FREE WITH NEOPRENE LINED, SIZES XSMALL, SMALL, MEDIUM, LARGE, XLARGE PT. SHAMROCK MANUFACTURING CORP.
K030325 01/31/2003 POWDERFREE LATEX EXAMINATION GLOVES WITH BUBBLEGUM PT. SHAMROCK MANUFACTURING CORP.
K030560 02/21/2003 POWDERFREE LATEX EXAMINATION GLOVES WITH GRAPE PT. SHAMROCK MANUFACTURING CORP.
K081040 04/11/2008 POWDERED LATEX EXAMINATION GLOVES, SMALL, MEDIUM, LARGE, X-LARGE PT. SHAMROCK MANUFACTURING CORP.
K011712 06/04/2001 LATEX EXAMINATION GLOVES- POWDER FREE, BLUE PT. SHAMROCK MANUFACTURING CORP.
K052382 08/30/2005 POWDER FREE NITRILE EXAMINATION GLOVES, BLUE PT. SHAMROCK MANUFACTURING CORP.
K052709 09/29/2005 POWDER FREE LATEX EXAMINATION GLOVES, SIZES SMALL, MEDIUM, LARGE, X-LARGE PT. SHAMROCK MANUFACTURING CORP.


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