# K062555: Ebsensor Blood Glucose Monitoring System, Model EB-G

- Pathway: 510(k) (Traditional)
- Applicant: Visgeneer, Inc.
- Decided: Dec 27, 2006 after 119 days
- Product code: NBW (System, Test, Blood Glucose, Over The Counter)
- Device class: 2
- Regulation: 21 CFR 862.1345
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K043197 (2005). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043197: Onetouch Ultra, Induo and Ultrasmart Blood Glucose Monitoring System, Lifescan, Inc. (2005) Summary page 1.

## Most influential descendants
- K122181: Ebchek Blood Glucose Monitoring System (2013), 0 descendants of its own
- K091765: Ebcarryon Blood Glucose Monitoring System (2010), 0 descendants of its own

## Indications for use
The eBsensor Blood Glucose Monitoring System, eB-G is intended for the quantitative measurement of glucose in fresh capillary whole blood from the finger. Testing is done outside the body ( in vitro diagnostic use). It is indicated for use at home ( over the counter [OTC] ) by person with diabetes, or in clinical setting by health care professionals, as an aid to monitor the effectiveness of diabetes control.

Source page: https://510kreport.com/device/K062555
Methodology: https://510kreport.com/methodology