Medical Device Manufacturer · MY , Kawasan Perusahaan Seramik Chepor

At Glove Engineering Sdn. Bhd - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
1
Total
1
Cleared
0
Denied

At Glove Engineering Sdn. Bhd has 1 FDA 510(k) cleared medical devices. Based in Kawasan Perusahaan Seramik Chepor, MY.

Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by At Glove Engineering 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 - At Glove Engineering Sdn. Bhd
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