# K073507: Anchorage Access Kit

- Pathway: 510(k) (Traditional)
- Applicant: Epitek, Inc.
- Decided: Mar 5, 2008 after 83 days
- Product code: ODC (Endoscope Channel Accessory)
- 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
Longest line of descent: 1 generation back to K061216 (2006). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061216: Usgi Transport Endoscopic Guide, Usgi Medical (2006) Summary page 4.

## Indications for use
The Anchorage™ Access Kit facilitates percutaneous access in order to establish a guide through which surgical instruments or devices can be intubated.

Source page: https://510kreport.com/device/K073507
Methodology: https://510kreport.com/methodology