Woodside Biomedical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Woodside Biomedical, Inc. Neurology ✕
6 devices
Cleared
Mar 21, 2002
RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL
Neurology
62d
Cleared
Mar 16, 2000
RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL
Neurology
79d
Cleared
Dec 09, 1999
RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R
Neurology
401d
Cleared
Feb 23, 1999
RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-R
Neurology
182d
Cleared
Oct 08, 1998
RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-R
Neurology
86d
Cleared
Feb 18, 1998
RELIEFBAND
Neurology
21d