# K260892: Suction Pump (SU-90)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen HugeMed Medical Technical Development Co., Ltd.
- Decided: May 14, 2026 after 57 days
- Product code: BTA (Pump, Portable, Aspiration (Manual Or 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: 2 generations back to K011725 (2001). 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)
- K130123: Basic and Dominant Flex Suction Pumps, Medela AG (2013) Summary page 5.

## Indications for use
The SU-90 Suction Pump is indicated for vacuum extraction, aspiration during flexible endoscopy and aspiration and removal of surgical fluids, tissue(including bone), gases, bodily fluids or infectious materials from wounds or from a patient's airway or respiratory support system. Intended use in hospital environments.

Source page: https://510kreport.com/device/K260892
Methodology: https://510kreport.com/methodology