Medical Device Manufacturer · US , Lake Forest , CA

Woodside Biomedical, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

Recent clearances: RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL, RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL, RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R

View 6 510(k) Devices ↓

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Woodside Biomedical, Inc. Neurology ✕

6 devices

1-6 of 6

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

Neurology · 21d