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FDA 510(k)

On Call Express Mobile Blood Glucose Monitoring System

K-Number: K180196 · 2018-03-07

Decision Date2018-03-07
Product CodeNBW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

On Call Express Mobile Blood Glucose Monitoring System is a medical device manufactured by ACON Laboratories, Inc.. It received FDA 510(k) clearance on 2018-03-07 under approval number K180196. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the On Call Express Mobile Blood Glucose Monitoring System?

On Call Express Mobile Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2018-03-07. It is manufactured by ACON Laboratories, Inc.. The 510(k) number is K180196.

When was On Call Express Mobile Blood Glucose Monitoring System approved by the FDA?

On Call Express Mobile Blood Glucose Monitoring System received FDA 510(k) clearance on 2018-03-07, under approval number K180196.

What company makes On Call Express Mobile Blood Glucose Monitoring System?

On Call Express Mobile Blood Glucose Monitoring System is manufactured by ACON Laboratories, Inc..

What is the FDA product code for On Call Express Mobile Blood Glucose Monitoring System?

The FDA product code for On Call Express Mobile Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.

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Official Source

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