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Medlogic Global Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K083531LIQUIBAND ULTIMA, MODEL LB0004February 12, 2009
K993556LIQUIBAND DENTALJanuary 3, 2000
K972081SUPERSKINDecember 17, 1997