FDA 510(k) Applications Submitted by W.A. Rubbermate Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K971200 04/01/1997 W.A. W.A. RUBBERMATE CO., LTD.
K021041 04/01/2002 WA RUBBERMATE LATEX POWDER-FREE EXAM GLOVES W.A. RUBBERMATE CO., LTD.
K233740 11/22/2023 Black Nitrile Powder Free Patient Examination Glove, Non Sterile W.A. Rubbermate Co., Ltd.
K110418 02/14/2011 POWDER FREE NITRILE EXAMINATION GLOVES W.A. RUBBERMATE CO., LTD.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact