# K111986: Logic Laparoscopic Instrument System

- Pathway: 510(k) (Traditional)
- Applicant: Surgical Innovations Plc
- Decided: Jan 26, 2012 after 197 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The Logic Laparoscopic Instrument System, Electrosurgical, Culling & Coagulation & Accessories is designed to dissect, grasp, manipulate and/or cauterise various tissues during manual operations in minimally invasive surgery and general endloscopic/laparoscopic procedures.

Source page: https://510kreport.com/device/K111986
Methodology: https://510kreport.com/methodology