Supermax Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Supermax Sdn Bhd - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Supermax Sdn Bhd has 9 FDA 510(k) cleared medical devices. Based in Petaling Jaya, Selangor, MY.
Historical record: 9 cleared submissions from 1990 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Supermax Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Supermax Sdn Bhd
9 devices
Cleared
Mar 05, 2002
CHLORINATED POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES WITH ALOE VERA
General Hospital
112d
Cleared
Jan 20, 2000
COLORED AND FLAVORED POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
66d
Cleared
Jan 20, 2000
GREEN PEPPERMINT FLAVORED POWDERED LATEX EXAMINATION GLOVES
General Hospital
66d
Cleared
Oct 27, 1999
SUPERGLOVES, POWDER FREE NITRILE EXAMINATION GLOVES
General Hospital
28d
Cleared
May 26, 1999
SUPERGLOVES, POLYMER COATED POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
33d
Cleared
Jul 22, 1998
SUPERGLOVES POWDERED NITRILE
General Hospital
128d
Cleared
Jun 09, 1998
SUPERGLOVES
General Hospital
120d
Cleared
Jan 22, 1993
PATIENT EXAMINATION LATEX GLOVES, HYPOALLERGENIC
General Hospital
436d
Cleared
Jan 10, 1990
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
279d