# K072404: Erbe Erbejet 2 System

- Pathway: 510(k) (Abbreviated)
- Applicant: Erbe USA, Inc.
- Decided: Oct 31, 2007 after 65 days
- Product code: FQH (Lavage, Jet)
- Device class: 2
- Regulation: 21 CFR 880.5475
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K952726 (1995). 9 ancestors in all.
14 later devices descend from it; 3 cite it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033590: Erbe Helix Hydro-Jet, Erbe USA, Inc. (2004) Summary page 1.
- K022613: Helix Hydro-Jet, Erbe USA, Inc. (2002) Summary page 1.
- K012464: Helix Hydro-Jet, Andreas Pein Medizintechnik GmbH (2001) Summary page 1.

## Most influential descendants
- K083608: Erbe Hybrid Knife (2009), 13 descendants of its own
- K143306: ERBE WaterJet Model ERBEJET® 2 System with HybridAPC Probe (2015), 12 descendants of its own
- K171158: Single Use Electrosurgical knife (2017), 7 descendants of its own
- K243120: HybridAPC probe (2025), 1 descendant of its own
- K231023: ERBEJET® 2 System (2023), 1 descendant of its own

## Indications for use
The ERBEJET® 2 System is intended for the cutting and dissection of soft tissue in neurosurgery and soft tissue such as the liver, kidney, etc. within the abdomen, including Total Mesorectal Excision (TME), in open as well as endoscopic surgery.

Source page: https://510kreport.com/device/K072404
Methodology: https://510kreport.com/methodology