# K182013: EasyInstruments

- Pathway: 510(k) (Traditional)
- Applicant: Agency For Medical Innovations GmbH
- Decided: Mar 11, 2019 after 227 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
Longest line of descent: 4 generations back to K935270 (1994). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962119: RE-New Laparoscopic Instruments, Microline Pentax, Inc. (1996) Summary page 5.
- K160706: ReNew V Handpiece Laparoscopic Instruments, Microline Surgical, Inc. (2016) Summary page 5.
- K163615: Snowden-Pencer MicroLap 3mm Laparoscopic Instruments, Carefusion 2200, Inc. (2017) Summary page 5.

## Indications for use
The Easylnstruments are indicated for cutting, grasping, dissecting and coagulation of tissue in laparoscopic surgical procedures.

Source page: https://510kreport.com/device/K182013
Methodology: https://510kreport.com/methodology