# K931111: Endopath Disposable Flexible Surgical Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Ethicon Endo-Surgery, Inc.
- Decided: Jun 22, 1993 after 110 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K992288: Auto Suture* Soft Thoracoport** Obturator and Sleeve (1999), 0 descendants of its own
- K970888: Iotec Trocar and Flexible Cannula (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K931111
Methodology: https://510kreport.com/methodology