# K962863: Karl Storz Model 264305-20 Electronic Endoflator

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Nov 19, 1996 after 119 days
- Product code: HIF (Insufflator, Laparoscopic)
- Device class: 2
- Regulation: 21 CFR 884.1730
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K080852: Ksea Electronic CO2 Endoflator LC, Model 26430320-1 (2009), 0 descendants of its own

## Indications for use
The Karl Storz Model 264305 20 Electronic Endoflator is designed to facilitate the use of laparoscopes by distending the abdomen with CO, gas during laparoscopic surgical and diagnostic procedures.

Source page: https://510kreport.com/device/K962863
Methodology: https://510kreport.com/methodology