# K974139: Lquet Cannula/Trocar System

- Pathway: 510(k) (Traditional)
- Applicant: Lifequest Endoscopic Technologies, Inc.
- Decided: Jan 28, 1998 after 86 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: 1 generation back to K942703 (1994). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K942703: GM Reusable and Disposable Trocar and GM Reusable and Disposable Ultra-Light Cannula, Gm Engineering, Inc. (1994) Summary page 1.
- K944103: Laparoscopic/Endoscopic Instrument, Gabris Surgical Corp. (1994) Summary page 1.

## Indications for use
The LQET Cannula/Trocar System provides access for instruments during laproscopic/endoscopic surgical procedures.

Source page: https://510kreport.com/device/K974139
Methodology: https://510kreport.com/methodology