Durio Ppe Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Durio Ppe Sdn Bhd - FDA 510(k) Cleared Devices
Recent clearances: Durio Surgical Face Mask, Models 501 (3-ply, blue) and 545 (4-ply,blue)
1
Total
1
Cleared
0
Denied
Durio Ppe Sdn Bhd has 1 FDA 510(k) cleared medical devices. Based in Johor Bahru, MY.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Durio Ppe Sdn Bhd Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo by UL as regulatory consultant.
FDA 510(k) Regulatory Record - Durio Ppe Sdn Bhd
1 devices