Influx Pacific Sdn. Bhd. is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Influx Pacific Sdn. Bhd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Influx Pacific Sdn. Bhd. has 5 FDA 510(k) cleared medical devices. Based in Malacca, West Malaysia, MY.
Historical record: 5 cleared submissions from 1989 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Influx Pacific Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Influx Pacific Sdn. Bhd.
5 devices
Cleared
Mar 13, 1998
NITRILE EXAMINATION GLOVES - POWDER FREE
General Hospital
31d
Cleared
Sep 26, 1997
NITRILE EXAMINATION GLOVES-PRE POWDERED
General Hospital
253d
Cleared
Aug 25, 1993
POWDER-FREE LATEX EXAMINATION GLOVES
General Hospital
211d
Cleared
Jul 22, 1991
SURGICAL GLOVES
General Hospital
140d
Cleared
Jul 31, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
133d