Woodside Biomedical, Inc.
Woodside Biomedical, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2002.
Top product codes for Woodside Biomedical, Inc.
Recent clearances by Woodside Biomedical, Inc.
- K020180 — RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL
- K994387 — RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL
- K983907 — RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R
- K982967 — RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-R
- K982436 — RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-R
- K980333 — RELIEFBAND
Data sourced from openFDA. This site is unofficial and independent of the FDA.