# K100929: Unimom Allegro

- Pathway: 510(k) (Traditional)
- Applicant: Blue Egg CO
- Decided: Jun 16, 2010 after 72 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: 3 generations back to K801862 (1980). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053052: Medela Swing Breast Pump, Medela AG (2006) Summary page 1.
- K901344: Medela Battery Operated Breast Pump, Medela, Inc. (1990) Summary page 1.

## Indications for use
The Unimom Allegro is intended to express breast milk from the breast of a lactating woman.

Source page: https://510kreport.com/device/K100929
Methodology: https://510kreport.com/methodology