# K081463: Mebby Gentlefeed Duo Breast Pump/Dual Expresser Pump

- Pathway: 510(k) (Abbreviated)
- Applicant: Medel S.P.A.
- Decided: Feb 6, 2009 after 259 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Intended Use of the GENTLEFEED DUO BREAST PUMP is.to express milk from the breast-of lactating women.

Source page: https://510kreport.com/device/K081463
Methodology: https://510kreport.com/methodology