FDA 510(k) Applications Submitted by GREAT GLOVE SDN BHD

FDA 510(k) Number Submission Date Device Name Applicant
K993386 10/08/1999 LATEX EXAMINATION POWDERED GLOVES GREAT GLOVE SDN BHD
K052955 10/21/2005 NITRILE BLUE POWDERED EXAMINATION GLOVES GREAT GLOVE SDN BHD
K052956 10/21/2005 NITRILE BLUE POWDER FREE EXAMINATION GLOVE GREAT GLOVE SDN BHD
K020363 02/04/2002 GREAT GLOVE LATEX EXAMINATION POWDERFREE GLOVES WITH PROTEIN LABELLING CLAIMS (50 MICROGRAMS OR LESS) GREAT GLOVE SDN BHD


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