Glovmaster Sdn. Bhd. is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Glovmaster Sdn. Bhd. - FDA 510(k) Cleared Devices
Recent clearances: Glovmaster Nitrile Examination Glove Powder Free
1
Total
1
Cleared
0
Denied
Glovmaster Sdn. Bhd. has 1 FDA 510(k) cleared medical devices. Based in Banting, MY.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Glovmaster Sdn. Bhd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Liberty Management Group Limited as regulatory consultant.
FDA 510(k) Regulatory Record - Glovmaster Sdn. Bhd.
1 devices