POGO Automatic Blood Glucose Monitoring System
K-Number: K162203 · 2017-04-06
Device Summary
Frequently Asked Questions
What is the POGO Automatic Blood Glucose Monitoring System?
POGO Automatic Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2017-04-06. It is manufactured by Intuity Medical, Inc.. The 510(k) number is K162203.
When was POGO Automatic Blood Glucose Monitoring System approved by the FDA?
POGO Automatic Blood Glucose Monitoring System received FDA 510(k) clearance on 2017-04-06, under approval number K162203.
What company makes POGO Automatic Blood Glucose Monitoring System?
POGO Automatic Blood Glucose Monitoring System is manufactured by Intuity Medical, Inc..
What is the FDA product code for POGO Automatic Blood Glucose Monitoring System?
The FDA product code for POGO Automatic Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.
Related Clinical Trials
Related PubMed Literature
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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.