Transcorp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Transcorp - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Transcorp has 6 FDA 510(k) cleared medical devices. Based in Chester, US.
Historical record: 6 cleared submissions from 1989 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Transcorp Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Transcorp
6 devices
Cleared
May 13, 1993
LATEX EXAMINATION GLOVES
General Hospital
356d
Cleared
Feb 27, 1992
STERILETX POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
101d
Cleared
Jan 11, 1991
SRI JOHANI LATEX SURGEONS GLOVES
General Hospital
88d
Cleared
Aug 07, 1990
KLEARTEX LATEX SURGICAL GLOVES
General Hospital
26d
Cleared
Aug 24, 1989
MEDPRIDE LATEX EXAMINATION GLOVES
General Hospital
34d
Cleared
Mar 24, 1989
TEXMED LATEX EXAMINATION GLOVE
General Hospital
22d