# K936231: The Karl Storz Hamou Endomat

- Pathway: 510(k) (Traditional)
- Applicant: Karl Storz Endoscopy
- Decided: Jan 24, 1995 after 391 days
- Product code: HIG (Insufflator, Hysteroscopic)
- Device class: 2
- Regulation: 21 CFR 884.1700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
22 later devices descend from it; 4 cite it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K022449: Hystereoscopy Pump HM4 (2003), 20 descendants of its own
- K031616: Iur Fluid Management System (2003), 15 descendants of its own
- K112642: Aquilex Fluid Control System H112 (2012), 14 descendants of its own
- K123732: Hysteroscopy Pump HM6 (2013), 6 descendants of its own
- K190372: Aveta System (2019), 4 descendants of its own

Source page: https://510kreport.com/device/K936231
Methodology: https://510kreport.com/methodology