Medical Device Manufacturer · MY , Tiga Lama Klang Sl

Tegas Setia Sdn Bhd - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1989

Total

Cleared

Denied

Tegas Setia Sdn Bhd has 1 FDA 510(k) cleared medical devices. Based in Tiga Lama Klang Sl, MY.

Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Tegas Setia Sdn Bhd Filter by specialty or product code using the sidebar.

Tegas Setia Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tegas Setia Sdn Bhd

1 devices

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