Perusahaan Pelindung Getah (M) Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Perusahaan Pelindung Getah (M) Sdn Bhd - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Perusahaan Pelindung Getah (M) Sdn Bhd has 8 FDA 510(k) cleared medical devices. Based in Seremban, N.S., MY.
Historical record: 8 cleared submissions from 1989 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Perusahaan Pelindung Getah (M) Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Perusahaan Pelindung Getah (M) Sdn Bhd
8 devices
Cleared
May 16, 2008
POWDER FREE NATURAL RUBBER LOW MODULUS LATEX PATIENT EXAMINATION GLOVES WITH...
General Hospital
273d
Cleared
Oct 10, 2003
RUBBERCARE POWDERED LATEX EXAMINATION GLOVES
General Hospital
84d
Cleared
Sep 08, 2000
RUBBERCARE POLYMER-COATED POWDERED LATEX EXAMINATION GLOVES/GUARDIAN...
General Hospital
58d
Cleared
Aug 14, 2000
RUBBERCARE POLYMER-CHLORINATED POWDER-FREE GUARDIAN POLYMER-CHLORINATED...
General Hospital
33d
Cleared
Aug 11, 2000
RUBBERCARE GUARDIAN POLYMER-COATED POWDER-FREE LATEX EXAMINATION GLOVES:...
General Hospital
30d
Cleared
Feb 07, 2000
RUBBERCARE POWDER-FREE, GUARDIAN POWDER-FREE LATEX EXAM GLOVES WITH PROTEIN...
General Hospital
56d
Cleared
Mar 21, 1994
RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED
General Hospital
243d
Cleared
Jul 14, 1989
RUBBERCARE PATIENT EXAMINATION GLOVE
General Hospital
134d