Vivachek Laboratories, Inc. is one of 13019 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vivachek Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VivaChek Ino Smart Blood Glucose Monitoring System, VivaChek Ino Sync Blood Glucose Monitoring System, VivaChek Ino Sound Blood Glucose Monitoring System, VivaChek Ino Plus Blood Glucose Monitoring System, VivaChek Ino Sound Simple Blood Glucose Monitoring System, VivaChek Ino Sound Bright Blood Glucose Monitoring System, VivaChek Ino Blood Glucose Monitoring System
2
Total
2
Cleared
0
Denied
Vivachek Laboratories, Inc. has 2 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Historical record: 2 cleared submissions from 2017 to 2018. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Vivachek Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vivachek Laboratories, Inc.
2 devices