# K140031: Suction Pump

- Pathway: 510(k) (Traditional)
- Applicant: Ding Hwa Co., Ltd.
- Decided: Apr 28, 2014 after 112 days
- Product code: JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 878.4780
- 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 K944399 (1995). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112421: Emg Suction Unit, Emg Technology Co., Ltd. (2011) Summary page 1.

## Indications for use
AS-XXXX Suction Pump is intended to be used to remove bodily fluids from a patient's airway or respiratory system.

Source page: https://510kreport.com/device/K140031
Methodology: https://510kreport.com/methodology