# K820159: Pressure Infuser

- Pathway: 510(k) (Traditional)
- Applicant: David Clark Company, Inc.
- Decided: Apr 21, 1982 after 91 days
- Product code: KZD (Infusor, Pressure, For I.V. Bags)
- Device class: 1
- Regulation: 21 CFR 880.5420
- 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
- K090736: Power Infuser, Model M100B-3A (2009), 1 descendant of its own
- K172653: Power Infuser (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K820159
Methodology: https://510kreport.com/methodology