Meridian Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Meridian Co., Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Meridian Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Songpa-Gu, Seoul, KR.
Historical record: 7 cleared submissions from 2000 to 2011. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Meridian Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meridian Co., Ltd.
7 devices
Cleared
Feb 25, 2011
LUCIA
Physical Medicine
189d
Cleared
Dec 29, 2008
LAPEX BCS
Physical Medicine
173d
Cleared
Jan 21, 2005
LAPEX 2000
Physical Medicine
394d
Cleared
Feb 19, 2003
MCPULSE
Cardiovascular
145d
Cleared
Aug 29, 2002
ABR-2000
Neurology
206d
Cleared
Jun 19, 2001
MERIDIAN-PORTABLE
Neurology
85d
Cleared
Nov 03, 2000
MERIDIAN-II AND MERDIAN-PLUS
Neurology
189d