Ampri Rubberware Industries Sdn Bhd is one of 141 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Ampri Rubberware Industries Sdn Bhd - FDA 510(k) Cleared Devices
Recent clearances: ABSOGEL CHEMOTHERAPHY GLOVES, POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTA, AMPRI
8
Total
8
Cleared
0
Denied
Ampri Rubberware Industries Sdn Bhd has 8 FDA 510(k) cleared medical devices. Based in Lumpur, Malaysia, MY.
Historical record: 8 cleared submissions from 1989 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ampri Rubberware Industries Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ampri Rubberware Industries Sdn Bhd
8 devices
Cleared
Nov 01, 1999
ABSOGEL CHEMOTHERAPHY GLOVES
General Hospital
244d
Cleared
May 04, 1999
POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (CONTAINS 50...
General Hospital
54d
Cleared
Jan 29, 1996
AMPRI
General Hospital
157d
Cleared
Sep 05, 1995
AMPRI
General Hospital
77d
Cleared
Jul 31, 1995
ABSOGEL STERILE POWDER-FREE SURGICAL GLOVES
General Hospital
237d
Cleared
Jul 20, 1995
ABSOGEL NON-STERILE EXAMINATION GLOVES (POWDER-FREE)
General Hospital
226d
Cleared
Sep 06, 1989
CORRECT TOUCH SURGEONS GLOVES
General Hospital
154d
Cleared
Aug 25, 1989
CORRECT TOUCH EXAMINATION GLOVES (LATEX)
General Hospital
142d