R.H. Burton Co. - FDA 510(k) Cleared Devices
Recent clearances: BURTON H- BASE TABLE - MODEL 1990, BURTON AUTOMATIC PROJECTOR - MODEL CP-40, BURTON SLIT LAMP - MODEL 850
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - R.H. Burton Co. Orthopedic ✕
1 devices