Medical Device Manufacturer · US , Tucson , AZ

Xeridiem (Formerly Mri) - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Xeridiem (Formerly Mri) has 2 FDA 510(k) cleared medical devices. Based in Tucson, US.

Historical record: 2 cleared submissions from 2015 to 2015. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Xeridiem (Formerly Mri) Filter by specialty or product code using the sidebar.

Xeridiem (Formerly Mri) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Xeridiem (Formerly Mri)

2 devices

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