CONTOUR® PLUS BLUE Blood Glucose Monitoring System
K-Number: K231679 · 2024-02-23
Device Summary
Frequently Asked Questions
What is the CONTOUR® PLUS BLUE Blood Glucose Monitoring System?
CONTOUR® PLUS BLUE Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2024-02-23. It is manufactured by Ascensia Diabetes Care. The 510(k) number is K231679.
When was CONTOUR® PLUS BLUE Blood Glucose Monitoring System approved by the FDA?
CONTOUR® PLUS BLUE Blood Glucose Monitoring System received FDA 510(k) clearance on 2024-02-23, under approval number K231679.
What company makes CONTOUR® PLUS BLUE Blood Glucose Monitoring System?
CONTOUR® PLUS BLUE Blood Glucose Monitoring System is manufactured by Ascensia Diabetes Care.
What is the FDA product code for CONTOUR® PLUS BLUE Blood Glucose Monitoring System?
The FDA product code for CONTOUR® PLUS BLUE 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.