Supermax Glove Manufacturing Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Supermax Glove Manufacturing Sdn Bhd - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Supermax Glove Manufacturing Sdn Bhd has 6 FDA 510(k) cleared medical devices. Based in Selangor, MY.
Historical record: 6 cleared submissions from 2000 to 2003. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Supermax Glove Manufacturing Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Supermax Glove Manufacturing Sdn Bhd
6 devices
Cleared
Jan 10, 2003
GREEN POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES WITH PEPPERMINT FLAVOR
General Hospital
30d
Cleared
Mar 13, 2002
STERILE POWDER FREE LATEX SURGEON GLOVES WITH PROTEIN LABELING CLAIM (50...
General Hospital
77d
Cleared
Feb 26, 2002
AURELIA CHLORINATED POWDER FREE LATEX MEDICAL EXAMINATION GLOVES WITH ALOE...
General Hospital
88d
Cleared
Jan 08, 2002
CHLORINATED POWDER FREE LATEX MEDICAL EXAMINATION GLOVES WITH ALOE VERA
General Hospital
70d
Cleared
Feb 23, 2001
STERILE POWDERED LATEX SURGEON GLOVES
General Hospital
32d
Cleared
Mar 17, 2000
SUPERGLOVES STERILE POWDERED LATEX EXAMINATION GLOVES
General Hospital
21d