# K951739: Pump/Blood Chemistry Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Via Medical Corp.
- Decided: Feb 28, 1996 after 320 days
- Product code: LZF (Pump, Infusion, Analytical Sampling)
- Device class: 2
- Regulation: 21 CFR 880.5725
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K162042: OptiScanner 5000 Glucose Monitoring System (2017), 1 descendant of its own
- K192785: OptiScanner® 5000 Glucose Monitoring System (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K951739
Methodology: https://510kreport.com/methodology