Brightway Gloves Pvt. , Ltd. is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Brightway Gloves Pvt. , Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Brightway Gloves Pvt. , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Tamil Nadu, IN.
Historical record: 4 cleared submissions from 2002 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Brightway Gloves Pvt. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Brightway Gloves Pvt. , Ltd.
4 devices
Cleared
May 22, 2002
LATEX SURGEONS GLOVE (POWDER FREE)
General Hospital
146d
Cleared
May 14, 2002
LATEX SURGEONS GLOVE (POWDERED)
General Hospital
138d
Cleared
Mar 20, 2002
LATEX EXAMINATION GLOVES (POWDER FREE)
General Hospital
83d
Cleared
Mar 20, 2002
LATEX EXAMINATION GLOVE (POWDERED)
General Hospital
83d