# K061216: Usgi Transport Endoscopic Guide

- Pathway: 510(k) (Special)
- Applicant: Usgi Medical
- Decided: May 15, 2006 after 13 days
- Product code: FED (Endoscopic Access Overtube, Gastroenterology-Urology)
- 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K073507: Anchorage Access Kit (2008), 0 descendants of its own
- K072405: Usgi Transport Endoscopic Access Device (2007), 0 descendants of its own

## Indications for use
The USGI TransPort Endoscopic Guide is intended to be used with an endoscope to facilitate intubation of the endoscope and as a guide for various flexible endoscopic instruments.

Source page: https://510kreport.com/device/K061216
Methodology: https://510kreport.com/methodology