Medipure Corporation (M) Sdn. Bhd. is one of 368 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Medipure Corporation (M) Sdn. Bhd. - FDA 510(k) Cleared Devices
Recent clearances: POWDER FREE LATEX EXAMINATION GLOVES, NATURAL OR BLUE COLOUR AND WITH PROTEIN CONTENT LABELING CLAIM (50 UG OR LESS), POLYMER COATED POWDER FREE, LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)
2
Total
2
Cleared
0
Denied
Medipure Corporation (M) Sdn. Bhd. has 2 FDA 510(k) cleared medical devices. Based in Kuala Kangsar, Perak, MY.
Historical record: 2 cleared submissions from 2000 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medipure Corporation (M) Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medipure Corporation (M) Sdn. Bhd.
2 devices