Ar Alliance Healthcare Sdn. Bhd. is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Ar Alliance Healthcare Sdn. Bhd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Ar Alliance Healthcare Sdn. Bhd. has 4 FDA 510(k) cleared medical devices. Based in Nibong Tebal, Pulau Pinang, MY.
Historical record: 4 cleared submissions from 2002 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ar Alliance Healthcare Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ar Alliance Healthcare Sdn. Bhd.
4 devices
Cleared
Nov 08, 2002
NITRI GRIP POWDERED NITRILE EXAMINATION GLOVES
General Hospital
98d
Cleared
Sep 06, 2002
POWDER FREE NITRILE EXAMINATION GLOVES
General Hospital
30d
Cleared
Apr 23, 2002
ULTRA TOUCH POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM...
General Hospital
40d
Cleared
Mar 06, 2002
ULTRA TOUCH POWDERED LATEX EXAMINATION GLOVES
General Hospital
30d