FDA 510(k) Applications Submitted by WOODSIDE BIOMEDICAL, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K020180 |
01/18/2002 |
RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL |
WOODSIDE BIOMEDICAL, INC. |
K980333 |
01/28/1998 |
RELIEFBAND |
WOODSIDE BIOMEDICAL, INC. |
K982436 |
07/14/1998 |
RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-R |
WOODSIDE BIOMEDICAL, INC. |
K982967 |
08/25/1998 |
RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-R |
WOODSIDE BIOMEDICAL, INC. |
K994387 |
12/28/1999 |
RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL |
WOODSIDE BIOMEDICAL, INC. |
K983907 |
11/03/1998 |
RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R |
WOODSIDE BIOMEDICAL, INC. |
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