FDA 510(k) Applications Submitted by XERIDIEM (FORMERLY MRI)

FDA 510(k) Number Submission Date Device Name Applicant
K142075 07/31/2014 BI-FUNNEL GASTROSTOMY FEEDING TUBE, TRI-FUNNEL GASTROSTOMY FEEDING TUBE XERIDIEM (FORMERLY MRI)
K142297 08/18/2014 Endo Vive 3S Low Profile Balloon Kit, Endo Vive 3S Bolus Extension Sets, Endo Vive 3S Continuous Extension Sets, Endo Vive 3S Medication Extension Set XERIDIEM (FORMERLY MRI)


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