Medical Device Manufacturer · MY , Taiping, Perak

Latexx Manufacturing Sdn.Bhd. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2002

Recent clearances: POWDER FREE NITRLE EXAMINATION GLOVES WITH CHEMOTHERAPY LABELING CLAIM, NON-CHLORINATED, POLYMER COATED POWDER FREE NATURAL RUBBER LATEX EXAMINATION GLOVES AND PROTEIN LABELING CLAIM OF, BLACK COLOUR POWDER-FREE NITRILE RUBBER EXAMINATION GLOVES

10
Total
10
Cleared
0
Denied

Latexx Manufacturing Sdn.Bhd. has 10 FDA 510(k) cleared general hospital devices. Based in Taiping, Perak, MY.

Historical record: 10 cleared submissions from 2002 to 2012.

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 - Latexx Manufacturing Sdn.Bhd.

10 devices
1-10 of 10
Filters
All10 General Hospital 10