Newlife Sciences, LLC is one of 24162 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Newlife Sciences, LLC - FDA 510(k) Cleared Devices
Recent clearances: NEWLIFE SCIENCES LLC, MODEL TMR
1
Total
1
Cleared
0
Denied
Newlife Sciences, LLC has 1 FDA 510(k) cleared medical devices. Based in Merrimack, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Newlife Sciences, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Newlife Sciences, LLC
1 devices