# K093635: Models Fora V30 and TD-4242 Blood Glucose Monitoring Systems

- Pathway: 510(k) (Special)
- Applicant: Taidoc Technology Corporation
- Decided: Feb 18, 2010 after 87 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: 2 generations back to K070472 (2007). 2 ancestors in all.
1 later device descends from it; 1 cites 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)
- K090187: Fora G30 Blood Glucose Monitoring System, Model TD-4241, Taidoc Technology Corporation (2009) Summary page 2.

## Most influential descendants
- K112275: Fora Premium V10 Blood Glucose Monitoring System (2011), 0 descendants of its own

## Indications for use
The FORA V30 Blood Glucose Monitoring System/TD-4242 Blood Glucose Monitoring System are intended for use in the quantitative measurement of glucose in fresh capillary whole blood from the finger and the following alternative sites: the palm, the forearm, the upper-arm, the calf and the thigh. It is intended for use by healthcare professionals and people with diabetes mellitus at home as an aid in monitoring the effectiveness of diabetes control program. It is not intended for the diagnosis of or screening for diabetes mellitus, and is not intended for use on neonates. The alternative site testing in the FORA V30 Blood Glucose Monitoring System /TD-4242 Blood Glucose Monitoring System can be used only during steady-state blood glucose conditions. This meter has some speaking functions but is not intended for use by the visually impaired.

Source page: https://510kreport.com/device/K093635
Methodology: https://510kreport.com/methodology