# K182749: Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump

- Pathway: 510(k) (Traditional)
- Applicant: Lansinoh Laboratories Saglik Gerecleri Tasarim San. Tic., Ltd.
- Decided: Jun 12, 2019 after 257 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: 5 generations back to K801862 (1980). 9 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122474: Lansinoh Powered Electric Breast Pump, Lansinoh Laboratories Saglik Gerecleri Tasarim San (2012) Summary page 5.

## Most influential descendants
- K222726: Smartpump 3.0 Double Electric Breast Pump (2022), 1 descendant of its own
- K230469: Compact Wearable Pump (2023), 0 descendants of its own

## Indications for use
The Lansinoh® Signature Pro™ Double Electric Breast Pump is intended to express and collect the breastmilk of a nursing woman for the purpose of feeding collected breastmilk to a baby. The pump is intended for multiple users, and single users. The Lansinoh® Smartpump™ Double Electric Breast Pump is intended to express and collect the breastmilk of a nursing woman for the purpose of feeding collected breastmilk to a baby. The pump is intended for multiple users, and single users.

Source page: https://510kreport.com/device/K182749
Methodology: https://510kreport.com/methodology