Meridian Medical Systems, LLC is one of 19020 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meridian Medical Systems, LLC - FDA 510(k) Cleared Devices
Recent clearances: Paragon 2, Universal Digital Interface 2W, UDI 2W, UNIVERSAL DIGITAL INTERFACE 2, UDI 2
6
Total
6
Cleared
0
Denied
Meridian Medical Systems, LLC has 6 FDA 510(k) cleared medical devices. Based in Aurora, US.
Historical record: 6 cleared submissions from 2011 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Meridian Medical Systems, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meridian Medical Systems, LLC
6 devices
Cleared
Oct 21, 2016
Paragon 2
Radiology
24d
Cleared
Jan 30, 2015
Universal Digital Interface 2W, UDI 2W
Radiology
81d
Cleared
Oct 22, 2014
UNIVERSAL DIGITAL INTERFACE 2, UDI 2
Radiology
264d
Cleared
May 22, 2012
UNIVERSAL DIGITAL INTERFACE (UDI) 1717
Radiology
265d
Cleared
Jan 31, 2012
UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W
Radiology
267d
Cleared
Apr 27, 2011
UNIVERSAL DIGITAL INTERFACE (UDI) 1717
Radiology
140d