W.A. Rubbermate Co., Ltd.

W.A. Rubbermate Co., Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 1997, most recent 2024.

Top product codes for W.A. Rubbermate Co., Ltd.

LYY — General Hospital2 devices
LZA — General Hospital2 devices

Recent clearances by W.A. Rubbermate Co., Ltd.

K233740 — Black Nitrile Powder Free Patient Examination Glove, Non SterileCode LZA·2024-02-13
K110418 — POWDER FREE NITRILE EXAMINATION GLOVESCode LZA·2011-07-13
K021041 — WA RUBBERMATE LATEX POWDER-FREE EXAM GLOVESCode LYY·2002-07-30
K971200 — W.A.Code LYY·1997-08-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.