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FDA 510(k) Applications Submitted by AMPRI RUBBERWARE INDUSTRIES SDN BHD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990677
03/02/1999
ABSOGEL CHEMOTHERAPHY GLOVES
AMPRI RUBBERWARE INDUSTRIES SDN BHD
K954002
08/25/1995
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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