# K130123: Basic and Dominant Flex Suction Pumps

- Pathway: 510(k) (Traditional)
- Applicant: Medela AG
- Decided: Oct 11, 2013 after 267 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: 1 generation back to K011725 (2001). 2 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021368: Medela Basic 30 and Dominant 50 Suction Pumps, Models 037, 057, Medela AG (2002) Summary page 3.
- K011725: Olympus Suction Pump, Model KV-5, Keymed (Medical & Industrial Equipment), Ltd. (2001) Summary page 3.

## Most influential descendants
- K150134: Basic, Dominant Flex, KV-6 (2015), 2 descendants of its own
- K260892: Suction Pump (SU-90) (2026), 0 descendants of its own
- K160950: Miniscav (2017), 0 descendants of its own
- K170329: Basic, Dominant Flex (2017), 0 descendants of its own

## Indications for use
The Basic and Dominant Flex Suction Pumps are 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 either during surgery or at the bedside.

Source page: https://510kreport.com/device/K130123
Methodology: https://510kreport.com/methodology