Sumirubber Industries (Kedah) Sdn. Bhd. is one of 175 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Sumirubber Industries (Kedah) Sdn. Bhd. - FDA 510(k) Cleared Devices
Recent clearances: NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDERED, NBR4 MILS NITRILE POWDER FREE EXAMINATION GLOVES NON-STERILE
3
Total
3
Cleared
0
Denied
Sumirubber Industries (Kedah) Sdn. Bhd. has 3 FDA 510(k) cleared medical devices. Based in Sungai Petani, Kedah, MY.
Historical record: 3 cleared submissions from 1989 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sumirubber Industries (Kedah) Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sumirubber Industries (Kedah) Sdn. Bhd.
3 devices