FDA 510(k) Applications Submitted by AMPRI RUBBERWARE INDUSTRIES SDN BHD

FDA 510(k) Number Submission Date Device Name Applicant
K892175 04/05/1989 CORRECT TOUCH EXAMINATION GLOVES (LATEX) AMPRI RUBBERWARE INDUSTRIES SDN BHD
K990677 03/02/1999 ABSOGEL CHEMOTHERAPHY GLOVES AMPRI RUBBERWARE INDUSTRIES SDN BHD
K892176 04/05/1989 CORRECT TOUCH SURGEONS GLOVES AMPRI RUBBERWARE INDUSTRIES SDN BHD
K954002 08/25/1995 AMPRI AMPRI RUBBERWARE INDUSTRIES SDN BHD
K945948 12/06/1994 ABSOGEL STERILE POWDER-FREE SURGICAL GLOVES AMPRI RUBBERWARE INDUSTRIES SDN BHD
K946056 12/06/1994 ABSOGEL NON-STERILE EXAMINATION GLOVES (POWDER-FREE) AMPRI RUBBERWARE INDUSTRIES SDN BHD
K952833 06/20/1995 AMPRI AMPRI RUBBERWARE INDUSTRIES SDN BHD
K990812 03/11/1999 POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTA AMPRI RUBBERWARE INDUSTRIES SDN BHD


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