The Newman Group, LLC is one of 24887 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Newman Group, LLC - FDA 510(k) Cleared Devices
Recent clearances: DIGDOP ULTRASOUND SYSTEM, BABYBEAT CORDLESS
2
Total
2
Cleared
0
Denied
The Newman Group, LLC has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 2 cleared submissions from 2006 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by The Newman Group, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - The Newman Group, LLC
2 devices