Cma Microdialysis AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cma Microdialysis AB - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cma Microdialysis AB has 4 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 4 cleared submissions from 2002 to 2011. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cma Microdialysis AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cma Microdialysis AB
4 devices
Cleared
Jan 14, 2011
MODIFICATION TO CMA CEREBRAL TISSUE MONITORING SYSTEM
Neurology
175d
Cleared
Jun 27, 2008
MODIFICATION TO CMA CEREBRAL TISSUE MONITORING SYSTEM
Neurology
344d
Cleared
May 02, 2006
CMA CEREBRAL TISSUE MONITORING SYSTEM
Neurology
62d
Cleared
Oct 23, 2002
CMA CEREBRAL TISSUE MONITORING SYSTEM
Neurology
268d