Hwa Teh Industrial Sdn. Bhd. is one of 9080 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hwa Teh Industrial Sdn. Bhd. - FDA 510(k) Cleared Devices
Recent clearances: HWA & SILKTEX POWDERED LATEX EXAMINATION GLOVES, WITH PROTEIN CONTENT LABELING CLAIM (140 MICROGRAMS OR LESS), HWA (AND) SILKTEX POWDER-FREE LATEX EXAMINATION GLOVE, HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE
6
Total
6
Cleared
0
Denied
Hwa Teh Industrial Sdn. Bhd. has 6 FDA 510(k) cleared medical devices. Based in Cerritos, US.
Historical record: 6 cleared submissions from 1989 to 2001. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hwa Teh Industrial Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hwa Teh Industrial Sdn. Bhd.
6 devices
Cleared
May 11, 2001
POWDER-FREE LATEX EXAMINATION GLOVES-BLUE COLOR
General Hospital
56d
Cleared
Apr 05, 2000
HWA (AND) SILKTEX POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING...
General Hospital
30d
Cleared
Feb 16, 2000
HWA & SILKTEX POWDERED LATEX EXAMINATION GLOVES, WITH PROTEIN CONTENT...
General Hospital
48d
Cleared
Sep 27, 1999
HWA (AND) SILKTEX POWDER-FREE LATEX EXAMINATION GLOVE
General Hospital
38d
Cleared
Sep 14, 1999
HWA (AND) SILKTEX PRE-POWDERED LATEX EXAMINATION GLOVE
General Hospital
32d
Cleared
Nov 21, 1989
HWA TEH EXAMINATION GLOVES
General Hospital
22d