Asia Pacific Latex Sdn Bhd - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Asia Pacific Latex Sdn Bhd has 4 FDA 510(k) cleared medical devices. Based in Darul Ridzuan, Malaysia, ML.
Historical record: 4 cleared submissions from 1994 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Asia Pacific Latex Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Asia Pacific Latex Sdn Bhd
4 devices
Cleared
Jan 28, 2004
ASIA PACIFIC LATEX SDN. BHD. POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
79d
Cleared
Jan 28, 2004
ASIA PACIFIC LATEX SDN. BHD. POLYMER COATED POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
79d
Cleared
Aug 11, 1998
NITRILE PATIENT EXAMINATION GLOVE POWDER FREE
General Hospital
43d
Cleared
Feb 03, 1994
LATEX PATIENT EXAMINATION GLOVES
General Hospital
527d