# K897096: Model 404A I.V. Infusion Pump Analyzer

- Pathway: 510(k) (Traditional)
- Applicant: Dynatech/Nevada, Inc.
- Decided: Mar 15, 1990 after 84 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.
3 later devices descend from it; 3 cite 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K961862: Models Ida-2 Plus and Ipt-1 (1997), 2 descendants of its own
- K980165: Infutest 2000 Infusion Device Analyzer (1998), 0 descendants of its own
- K973609: Ida-4 and Ipt-MC (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K897096
Methodology: https://510kreport.com/methodology