St. Marys Rubbers Pvt, Ltd. is one of 140 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
St. Marys Rubbers Pvt, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Medismart ( Latex Surgeon¿s Gloves powdered ) and Medismart + (Latex Surgeon¿s Gloves Powder Free, Polymer coated with protein
1
Total
1
Cleared
0
Denied
St. Marys Rubbers Pvt, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Kottayam District, Kerala, IN.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by St. Marys Rubbers Pvt, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by M/S Liberty Management Group, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - St. Marys Rubbers Pvt, Ltd.
1 devices