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

Woodside Biomedical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Lake Forest, US.

Historical record: 6 cleared submissions from 1998 to 2002. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Woodside Biomedical, Inc. Filter by specialty or product code using the sidebar.

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

6 devices
1-6 of 6
Cleared Mar 21, 2002
RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL
K020180 · GZJ
Neurology · 62d
Cleared Mar 16, 2000
RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL
K994387 · GZJ
Neurology · 79d
Cleared Dec 09, 1999
RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R
K983907 · GZJ
Neurology · 401d
Cleared Feb 23, 1999
RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-R
K982967 · GZJ
Neurology · 182d
Cleared Oct 08, 1998
RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-R
K982436 · GZJ
Neurology · 86d
Cleared Feb 18, 1998
RELIEFBAND
K980333 · GZJ
Neurology · 21d
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