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FDA 510(k) Applications Submitted by UNOMEDICAL SDN BHD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K962389
06/20/1996
EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE
UNOMEDICAL SDN BHD
K973076
08/18/1997
EUROMEDICAL HAEMATURIA FOLEY CATHETER
UNOMEDICAL SDN BHD
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