# K192921: Zeos Aqua Vision Pump and tube

- Pathway: 510(k) (Traditional)
- Applicant: Hemodia Sas
- Decided: Oct 9, 2020 after 359 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- 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 K954465 (1995). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130169: FMS Vue Fluid Managment System, FMS Connect Interface Cable, Depuy Mitek, A Johnson & Johnson Company (2013) Summary page 5.

## Most influential descendants
- K203480: DOUBLEFLO system (2021), 1 descendant of its own
- K221919: DOUBLEFLO INFLOW/OUTFLOW PUMP, accessories and tubing sets (2023), 0 descendants of its own

## Indications for use
The ZEOS AQUA VISION Pump is an arthroscopy pump system intended to provide fluid distension and irrigation of the knee, shoulder, hip, elbow, ankle and wrist joint cavities and fluid suction during arthroscopy procedures.

Source page: https://510kreport.com/device/K192921
Methodology: https://510kreport.com/methodology