FDA 510(k) Applications Submitted by GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD

FDA 510(k) Number Submission Date Device Name Applicant
K954967 10/30/1995 GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K010054 01/08/2001 GUTHRIE SHIELD BLUE LATEX EXAMINATION GLOVES, POWDERED WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS) GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K010078 01/10/2001 GUTHRIE SHIELD PLUS BLUE LATEX EXAMINATION GLOVES (POWDER-FREE) GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K000090 01/13/2000 GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K990228 01/25/1999 GUTHRIE PRIME POWDER-FREE GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K001047 03/31/2000 GUTHRIE LATEX SURGICAL GLOVE (PRE-POWDERED) GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K001049 03/31/2000 GUTHRIE POWDER-FREE LATEX SURGICAL GLOVE WITH (50 MICROGRAMS OR LESS) GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K993793 11/09/1999 GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K003872 12/15/2000 GUTHRIE PRIME POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS) GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K003922 12/20/2000 NITRILE EXAMINATION GLOVES (POWERED) GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD
K003985 12/26/2000 POWDERFREE NITRILE PATIENT EXMINATION GLOVE GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD


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