# K230469: Compact Wearable Pump

- Pathway: 510(k) (Traditional)
- Applicant: Lansinoh Laboratories
- Decided: Jun 30, 2023 after 129 days
- Product code: HGX (Pump, Breast, Powered)
- Device class: 2
- Regulation: 21 CFR 884.5160
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K801862 (1980). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222726: Smartpump 3.0 Double Electric Breast Pump, Lansinoh Laboratories (2022) Summary page 4.

## Indications for use
The Compact Wearable Pump is intended to express and collect breastmilk from lactating women for the purpose of feeding collected breastmilk to a baby. The Compact Wearable Pump is intended for a single user.

Source page: https://510kreport.com/device/K230469
Methodology: https://510kreport.com/methodology