Sriram Enterprises D.B.A. Momentum Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sriram Enterprises D.B.A. Momentum Group - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sriram Enterprises D.B.A. Momentum Group has 1 FDA 510(k) cleared medical devices. Based in Orlando, US.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Sriram Enterprises D.B.A. Momentum Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sriram Enterprises D.B.A. Momentum Group
1 devices