# K070255: Nova Max Blood Glucose Monitor System, 90001,90002

- Pathway: 510(k) (Traditional)
- Applicant: Nova Biomedical Corp.
- Decided: Jun 13, 2007 after 138 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
No predicates in its family tree.
16 later devices descend from it; 4 cite it directly.
1 of 17 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K091547: Nova Max Plus Blood Glucose and B-Ketone Monitor System, Nova Max Plus B-Ketone Control Solutions, Nova Max Blood Glucos (2010), 10 descendants of its own
- K112638: Nova Max One Blood Glucose Monitor, Nova Max One Blood Glucose Test Strips (2012), 3 descendants of its own
- K161738: FORA ADVANCED GD40 and FORA ADVANCED GD40 pro Blood Glucose and ß-Ketone Monitoring Systems (2016), 2 descendants of its own
- K170463: KetoSens Blood B-Ketone Monitoring System, KetoSens Multi Blood B-Ketone Monitoring System (2018), 1 descendant of its own
- K160156: StatStrip Xpress Blood Glucose Monitoring System (2016), 1 descendant of its own

Source page: https://510kreport.com/device/K070255
Methodology: https://510kreport.com/methodology