Ansell Malaysia Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Ansell Malaysia Sdn Bhd - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ansell Malaysia Sdn Bhd has 1 FDA 510(k) cleared medical devices. Based in Melaka, MY.
Historical record: 1 cleared submissions from 1995 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ansell Malaysia Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ansell Malaysia Sdn Bhd
1 devices