Pt.Shamrock Manufacturing Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pt.Shamrock Manufacturing Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Pt.Shamrock Manufacturing Corp. has 7 FDA 510(k) cleared medical devices. Based in City Of Industry, US.
Historical record: 7 cleared submissions from 2001 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pt.Shamrock Manufacturing Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pt.Shamrock Manufacturing Corp.
7 devices
Cleared
May 20, 2008
POWDERED LATEX EXAMINATION GLOVES, SMALL, MEDIUM, LARGE, X-LARGE
General Hospital
39d
Cleared
Nov 08, 2005
POWDER FREE LATEX EXAMINATION GLOVES, SIZES SMALL, MEDIUM, LARGE, X-LARGE
General Hospital
40d
Cleared
Sep 15, 2005
POWDER FREE NITRILE EXAMINATION GLOVES, BLUE
General Hospital
16d
Cleared
Mar 28, 2003
POWDERFREE LATEX EXAMINATION GLOVES WITH BUBBLEGUM
General Hospital
56d
Cleared
Mar 25, 2003
LATEX EXAMINATION GLOVES POWDER FREE WITH NEOPRENE LINED, SIZES XSMALL,...
General Hospital
70d
Cleared
Mar 21, 2003
POWDERFREE LATEX EXAMINATION GLOVES WITH GRAPE
General Hospital
28d
Cleared
Jul 17, 2001
LATEX EXAMINATION GLOVES- POWDER FREE, BLUE
General Hospital
43d