# K090404: Fore V10 Blood Glucose Monitoring System, Model TD-4244, Forea V12 Blodo Glucose Monitoring System, Model TD-4247

- Pathway: 510(k) (Special)
- Applicant: Taidoc Technology Corporation
- Decided: Jun 23, 2009 after 126 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have 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
- K093035: Fora V10 Blood Glucose Monitoring System, Model TD-4244 (2009), 1 descendant of its own
- K121706: Fora V10 Blood Glucose Monitoring System (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K090404
Methodology: https://510kreport.com/methodology