# K101631: Fora GD20 Blood Glucose Monitoring System, U-Rught TD-4252D Blood Glucose Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Taidoc Technology Corporation
- Decided: Sep 2, 2011 after 449 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; 2 cite 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K124040: Foracare GD20 Blood Glucose Monitoring System (2013), 0 descendants of its own
- K121224: Genesis Health Technologies Blood Glucose Monitoring System (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K101631
Methodology: https://510kreport.com/methodology