Rubberex Alliance Products Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Rubberex Alliance Products Sdn Bhd - FDA 510(k) Cleared Devices
Recent clearances: Non-Sterile Powder Free Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)
1
Total
1
Cleared
0
Denied
Rubberex Alliance Products Sdn Bhd has 1 FDA 510(k) cleared medical devices. Based in Ipoh, MY.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Rubberex Alliance Products Sdn Bhd Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Rubberex Alliance Products Sdn Bhd
1 devices