# K914589: Sabratek 3030 Infusion Pump

- Pathway: 510(k) (Traditional)
- Applicant: Sabratek Corp.
- Decided: May 18, 1992 after 215 days
- Product code: FRN (Pump, Infusion)
- 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; 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K993524: Advantis Asc Infusion Pump and Administration Sets (2000), 0 descendants of its own
- K980751: Sabratek 4040 Infusion Pump (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K914589
Methodology: https://510kreport.com/methodology