Mindchild Medical is one of 18376 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mindchild Medical - FDA 510(k) Cleared Devices
Recent clearances: Meridian M110 Fetal Monitoring System, MindChild Meridian M100 Fetal Heart Rate Monitor, MINDCHILD MERIDIAN FETAL HEART RATE MONITOR
3
Total
3
Cleared
0
Denied
Mindchild Medical has 3 FDA 510(k) cleared medical devices. Based in Providence, US.
Historical record: 3 cleared submissions from 2012 to 2017. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Mindchild Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Northstar Biomedical Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Mindchild Medical
3 devices