# K961694: Impact

- Pathway: 510(k) (Traditional)
- Applicant: Matrix Technologies Corp.
- Decided: Jun 21, 1996 after 51 days
- Product code: JQW (Station, Pipetting And Diluting, For Clinical Use)
- Device class: 1
- Regulation: 21 CFR 862.2750
- 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
- K023955: BD Viper Instrument (2003), 1 descendant of its own
- K052481: BD Viper System (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K961694
Methodology: https://510kreport.com/methodology