# K023219: Becton Dickinson Diabetes Software

- Pathway: 510(k) (Traditional)
- Applicant: Becton, Dickinson & CO
- Decided: Dec 6, 2002 after 71 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) WinGlucofacts: named in the summary without a submission number

## Most influential descendants
- K103115: Prodigy Diabetes Management Software (2011), 0 descendants of its own

## Indications for use
The BDTM Diabetes Software is intended for use as a data management tool for acceptance, transfer, display, storage, processing (e.g. averaging), reporting, and printing of patient blood glucose monitoring data. The device is intended for use with the BD Blood Glucose Monitoring Systems only.

Source page: https://510kreport.com/device/K023219
Methodology: https://510kreport.com/methodology