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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