FDA 510(k) Applications Submitted by ROBERT S KENNEDY

FDA 510(k) Number Submission Date Device Name Applicant
K894569 07/21/1989 MEDPRIDE LATEX EXAMINATION GLOVES TRANSCORP
K940256 01/21/1994 BIOSHIELD BLUE LATEX GLOVES CHESTER LABS, INC.
K910631 02/13/1991 SUNTEX STERILE EXAM GLOVES P.T. LATEXINDO PRAUTAMA
K900868 02/23/1990 STERILE LATEX EXAMINATION GLOVE SRI JOHANI SDN. BHD.
K900869 02/23/1990 NON-STERILE LATEX PROCEDURE GLOVE SRI JOHANI SDN. BHD.
K891120 03/02/1989 TEXMED LATEX EXAMINATION GLOVE TRANSCORP
K892478 04/07/1989 SAFETEX & SUNTEX PATIENT EXAMINATION GLOVES P.T. LATEXINDO PRAUTAMA
K922439 05/22/1992 LATEX EXAMINATION GLOVES TRANSCORP
K903069 07/12/1990 KLEARTEX LATEX SURGICAL GLOVES TRANSCORP
K895027 08/08/1989 MEDPRIDE LATEX SURGEONS GLOVES MEDPRIDE
K924265 08/24/1992 DOCTOR'S CHOICE LATEX EXAMINATION GLOVES CHESIRE LABORATORIES
K924266 08/24/1992 DOCTOR'S CHOICE POWDER FREE LATEX EXAM GLOVES CHESIRE LABORATORIES
K915189 11/18/1991 STERILETX POWDER FREE LATEX EXAMINATION GLOVES TRANSCORP
K940254 01/21/1994 BIOSHIELD BLUE POWDER FREE GLOVE CHESTER LABS, INC.


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