Contour® next GEN Blood Glucose Monitoring System
K-Number: K193407 · 2021-12-23
Device Summary
Frequently Asked Questions
What is the Contour® next GEN Blood Glucose Monitoring System?
Contour® next GEN Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2021-12-23. It is manufactured by Ascensia Diabetes Care. The 510(k) number is K193407.
When was Contour® next GEN Blood Glucose Monitoring System approved by the FDA?
Contour® next GEN Blood Glucose Monitoring System received FDA 510(k) clearance on 2021-12-23, under approval number K193407.
What company makes Contour® next GEN Blood Glucose Monitoring System?
Contour® next GEN Blood Glucose Monitoring System is manufactured by Ascensia Diabetes Care.
What is the FDA product code for Contour® next GEN Blood Glucose Monitoring System?
The FDA product code for Contour® next GEN Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.
Related Clinical Trials
Related PubMed Literature
Other Devices by Ascensia Diabetes Care
Related Devices (Code: NBW)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.