Brightsway Holdings Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Brightsway Holdings Sdn Bhd - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Brightsway Holdings Sdn Bhd has 4 FDA 510(k) cleared medical devices. Based in Klang Selangor Darul Ehsan, MY.
Historical record: 4 cleared submissions from 1999 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Brightsway Holdings Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Brightsway Holdings Sdn Bhd
4 devices
Cleared
Jul 26, 1999
BRIGHTWAY BRAND LATEX SURGICAL GLOVES - STERILE (POWDERED)
General Hospital
40d
Cleared
Jul 23, 1999
BRIGHTWAY BRAND LATEX SURGICAL GLOVES - STERILE (POWDER FREE)
General Hospital
37d
Cleared
Jun 23, 1999
BRIGHTWAY BRAND BLUE COLOR LATEX EXAMINATION GLOVE, POWDER FREE CONTAINING 50...
General Hospital
30d
Cleared
Jun 23, 1999
BRIGHTWAY BRAND BLUE COLOR LATEX EXAMINATION GLOVE, POWDERED CONTAINING 150...
General Hospital
30d