Iquum, Inc. is one of 4771 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iquum, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Iquum, Inc. has 3 FDA 510(k) cleared medical devices. Based in Marlborough, US.
Historical record: 3 cleared submissions from 2011 to 2016. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Iquum, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Iquum, Inc.
3 devices