Maxter Glove Manufacturing Sdn Bhd - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Maxter Glove Manufacturing Sdn Bhd has 9 FDA 510(k) cleared medical devices. Based in 41050 Klang, Selangor, MY.
Historical record: 9 cleared submissions from 2001 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Maxter Glove Manufacturing Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Maxter Glove Manufacturing Sdn Bhd
9 devices
Cleared
May 02, 2018
Non-Sterile Powder Free Blue Nitrile Examination Gloves Tested for Use with...
General Hospital
224d
Cleared
May 02, 2016
Powder Free Nitrile Examination Gloves Tested For Use With Chemotherapy Drugs
General Hospital
342d
Cleared
Feb 06, 2012
POWDER FREE NITRILE EXAMINATION GLOVES TESTED FOR USE WITH CHEMOTHERAPY DRUGS
General Hospital
110d
Cleared
Feb 24, 2004
MAXTER POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES
General Hospital
29d
Cleared
Oct 17, 2003
MAXTER STERILE POWDER FREE SURGICAL GLOVES
General Hospital
65d
Cleared
Oct 10, 2003
MAXTER STERILE POWDERED LATEX SURGICAL GLOVES
General Hospital
60d
Cleared
Jan 17, 2002
CHLORINATED POWDER FREE LATEX MEDICAL EXAMINATION GLOVES WITH PROTEIN...
General Hospital
87d
Cleared
Jan 17, 2002
POLYMER COATED POWDER FREE LATEX MEDICAL EXAMINATION GLOVES WITH PROTEIN...
General Hospital
84d
Cleared
Nov 29, 2001
POWDERED LATEX MEDICAL MEDICAL EXAMINATION GLOVES WITH 150 MICROGRAMS OR LESS...
General Hospital
43d