# K100045: OCTO

- Pathway: 510(k) (Traditional)
- Applicant: Dalim Surgnet Corporation
- Decided: Jun 25, 2010 after 168 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
Longest line of descent: 4 generations back to K010007 (2001). 7 ancestors in all.
5 later devices descend from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073719: Asc Triport Laparoscopic Access Device, Advanced Surgical Concepts (2008) Summary page 1.

## Most influential descendants
- K112196: Octotmport (2011), 4 descendants of its own
- K141715: Glove Port (2015), 3 descendants of its own
- K233263: Disposable Trocars (2024), 0 descendants of its own
- K220081: Core-Sport (2022), 0 descendants of its own
- K152598: Endo Keeper (2016), 0 descendants of its own

## Indications for use
The OCTOm is intended for use as a multiple instrument and/or camera port during minimally invasive abdominal laparoscopic surgery.

Source page: https://510kreport.com/device/K100045
Methodology: https://510kreport.com/methodology