Slim River Latex Sdn. Bhd. is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Slim River Latex Sdn. Bhd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Slim River Latex Sdn. Bhd. has 4 FDA 510(k) cleared medical devices. Based in Perai, 13600 Perai, Malay, MY.
Historical record: 4 cleared submissions from 1990 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Slim River Latex Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Slim River Latex Sdn. Bhd.
4 devices
Cleared
Mar 15, 1994
SLIMFLEX - POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
257d
Cleared
Oct 05, 1993
POWDER-FREE EXAMINATION GLOVE
General Hospital
286d
Cleared
Nov 19, 1990
SLIMFLEX, PATIENT EXAMINATION GLOVES
General Hospital
12d
Cleared
Nov 08, 1990
PATIENT EXAMINATION GLOVES
General Hospital
7d