N.S. Uni-Gloves Sdn. Bhd. is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
N.S. Uni-Gloves Sdn. Bhd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
N.S. Uni-Gloves Sdn. Bhd. has 7 FDA 510(k) cleared medical devices. Based in Seremban N.S., MY.
Historical record: 7 cleared submissions from 1989 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by N.S. Uni-Gloves Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - N.S. Uni-Gloves Sdn. Bhd.
7 devices
Cleared
Apr 08, 2005
LANO-E POWDER-FREE NITRILE EXAMINATION GLOVE
General Hospital
15d
Cleared
Jan 22, 2002
UNIGLOVE LANO-E POWDER-FREE LATEX EXAMINATION GLOVES
General Hospital
123d
Cleared
May 16, 2001
UNIGLOVE POLYMER COATED POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN...
General Hospital
54d
Cleared
May 10, 2001
UNIGLOVE POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING...
General Hospital
48d
Cleared
Apr 28, 2000
UNIGLOVE NITRILE POWDER-FREE EXAMINATION GLOVES
General Hospital
59d
Cleared
Apr 12, 2000
UNIGLOVE NITRILE POWDERED EXAMINATION GLOVES
General Hospital
43d
Cleared
Apr 28, 1989
PATIENT EXAMINATION GLOVES
General Hospital
60d