Medical Device Manufacturer · US , St. Louis , MO

Institute For Quality Resource Management - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014
1
Total
1
Cleared
0
Denied

Institute For Quality Resource Management has 1 FDA 510(k) cleared medical devices. Based in St. Louis, US.

Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Institute For Quality Resource Management Filter by specialty or product code using the sidebar.

Institute For Quality Resource Management — FDA 510(k) Products and Clearance History

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