Robert R. Stevens is one of 15128 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Robert R. Stevens - FDA 510(k) Cleared Devices
Recent clearances: CUTANEOUS COMPRESSION DEVICE FOR USE IN HEMODIALYSIS, TAPE & BANDAGE, ADHESIVE
2
Total
2
Cleared
0
Denied
Robert R. Stevens has 2 FDA 510(k) cleared medical devices. Based in Miami Lakes, US.
Historical record: 2 cleared submissions from 1996 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Robert R. Stevens Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Robert R. Stevens
2 devices