Contour Next EZ Blood Glucose Monitoring System
K-Number: K162336 · 2017-01-12
Device Summary
Frequently Asked Questions
What is the Contour Next EZ Blood Glucose Monitoring System?
Contour Next EZ Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2017-01-12. It is manufactured by Ascensia Diabetes Care U.S., Inc.. The 510(k) number is K162336.
When was Contour Next EZ Blood Glucose Monitoring System approved by the FDA?
Contour Next EZ Blood Glucose Monitoring System received FDA 510(k) clearance on 2017-01-12, under approval number K162336.
What company makes Contour Next EZ Blood Glucose Monitoring System?
Contour Next EZ Blood Glucose Monitoring System is manufactured by Ascensia Diabetes Care U.S., Inc..
What is the FDA product code for Contour Next EZ Blood Glucose Monitoring System?
The FDA product code for Contour Next EZ 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 U.S., Inc.
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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.