Sri Anusham Rubber Industries Pvt., Ltd. is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Sri Anusham Rubber Industries Pvt., Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Sri Anusham Rubber Industries Pvt., Ltd. has 6 FDA 510(k) cleared medical devices. Based in India, IN.
Historical record: 6 cleared submissions from 1992 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sri Anusham Rubber Industries Pvt., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sri Anusham Rubber Industries Pvt., Ltd.
6 devices
Cleared
Nov 23, 1999
NIL, SURGEON'S GLOVE - POWDER FREE
General Hospital
49d
Cleared
Nov 19, 1999
NIL, NITRILE EXAMINATION GLOVE - POWDERED
General Hospital
45d
Cleared
Nov 19, 1999
NIL, NITRILE EXAMINATION GLOVE - POWDER FREE
General Hospital
45d
Cleared
May 21, 1999
SURGEON'S GLOVES
General Hospital
164d
Cleared
Jan 21, 1999
POWDER FREE LATEX EXAMINATION GLOVES
General Hospital
73d
Cleared
Apr 02, 1992
LATEX PATIENT EXAMINATION GLOVES
General Hospital
119d