FDA 510(k) Applications Submitted by UNOMEDICAL SDN BHD

FDA 510(k) Number Submission Date Device Name Applicant
K945806 11/28/1994 SILICATH ALL SILICONE FOLEY CATHETER UNOMEDICAL SDN BHD
K951696 04/12/1995 ENDOTRACHEAL TUBE UNOMEDICAL SDN BHD
K951697 04/12/1995 PEDIATRIC ENDOTRACHEAL TUBE UNOMEDICAL SDN BHD
K962389 06/20/1996 EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE UNOMEDICAL SDN BHD
K973076 08/18/1997 EUROMEDICAL HAEMATURIA FOLEY CATHETER UNOMEDICAL SDN BHD
K954750 10/16/1995 PEDIATRIC WIRE REINFORCED SILICONE ENDOTRACHEAL TUBE UNOMEDICAL SDN BHD
K954751 10/16/1995 SILICONE ENDOTRACHEAL TUBE UNOMEDICAL SDN BHD
K954753 10/16/1995 PEDIATRIC SILICONE ENDOTRACHEAL TUBE UNOMEDICAL SDN BHD
K954754 10/16/1995 WIRE REINFORCED SILICONE ENDOTRACHEAL TUBE UNOMEDICAL SDN BHD


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