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Mindchild Medical
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K161902
Meridian M110 Fetal Monitoring System
January 12, 2017
K142883
MindChild Meridian M100 Fetal Heart Rate Monitor
April 17, 2015
K120018
MINDCHILD MERIDIAN FETAL HEART RATE MONITOR
September 19, 2012