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Meridian Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
1
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K102375LUCIAFebruary 25, 2011
K081962LAPEX BCSDecember 29, 2008
K034009LAPEX 2000January 21, 2005
K023238MCPULSEFebruary 19, 2003
K020360ABR-2000August 29, 2002
K010897MERIDIAN-PORTABLEJune 19, 2001
K001347MERIDIAN-II AND MERDIAN-PLUSNovember 3, 2000