Elastic Care Incorporated is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Elastic Care Incorporated - FDA 510(k) Cleared Devices
Recent clearances: LifePath Remote Patient Monitoring Platform
1
Total
1
Cleared
0
Denied
Elastic Care Incorporated has 1 FDA 510(k) cleared medical devices. Based in Markham, CA.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Elastic Care Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Elastic Care Incorporated
1 devices