# K192640: Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump

- Pathway: 510(k) (Traditional)
- Applicant: Guangzhou Yongyi Industrial Co., Ltd.
- Decided: Mar 30, 2020 after 188 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: 4 generations back to K801862 (1980). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181937: Pump In Style Advanced, Advanced Personal Double Breastpump, Medela, LLC (2018) Summary page 4.

## Indications for use
The Kidro Digital Electric Breast Pump and Dr. Brown’s Digital Electric Breast Pump are powered breast pumps to be used by lactating women to express and collect milk from their breasts. They are intended for a single user.

Source page: https://510kreport.com/device/K192640
Methodology: https://510kreport.com/methodology