Iq Technologies, Inc. is one of 18392 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iq Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IQ Technologies, IQ TECHNOLOGIES
2
Total
2
Cleared
0
Denied
Iq Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Las Vegas, US.
Historical record: 2 cleared submissions from 2014 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Iq Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dr Certification, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Iq Technologies, Inc.
2 devices