Medical Device Manufacturer · MY , Kuala Lumpur

Tekmedic (M) Sdn Bhd - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1989

Recent clearances: POWDER FREE BLUE NITRILE EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS, COLORED POWDER FREE LATEX EXAMINATION GLOVE (WHITE AND BLUE), FLAVORED POWDER FREE AND POLYMER COATED EXAMINATION GLOVE (VANLLA, GRAPE AND STRAWBERRY)

11
Total
11
Cleared
0
Denied

Tekmedic (M) Sdn Bhd has 11 FDA 510(k) cleared general hospital devices. Based in Kuala Lumpur, MY.

Historical record: 11 cleared submissions from 1989 to 2013.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Tekmedic (M) Sdn Bhd

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