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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