K162336 is an FDA 510(k) clearance for the Contour Next EZ Blood Glucose Monitoring System. This device is classified as a System, Test, Blood Glucose, Over The Counter (Class II - Special Controls, product code NBW).
Submitted by Ascensia Diabetes Care U.S., Inc. (Mishawaka, US). The FDA issued a Cleared decision on January 12, 2017, 143 days after receiving the submission on August 22, 2016.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1345.
| 510(k) Number | K162336 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 22, 2016 |
| Decision Date | January 12, 2017 |
| Days to Decision | 143 days |
| Submission Type | Special |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | NBW - System, Test, Blood Glucose, Over The Counter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1345 |