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Mindchild Medical

FDA Regulatory Profile

Mindchild Medical appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 12, 2017.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K161902Meridian M110 Fetal Monitoring SystemJanuary 12, 2017
K142883MindChild Meridian M100 Fetal Heart Rate MonitorApril 17, 2015
K120018MINDCHILD MERIDIAN FETAL HEART RATE MONITORSeptember 19, 2012

FDA data resources