# K160706: ReNew V Handpiece Laparoscopic Instruments

- Pathway: 510(k) (Traditional)
- Applicant: Microline Surgical, Inc.
- Decided: Oct 19, 2016 after 219 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: 2 generations back to K932648 (1993). 2 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 5 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 4.

## Most influential descendants
- K182013: EasyInstruments (2019), 0 descendants of its own
- K171523: Monopolar Single Use Laparoscopic Instrument (2017), 0 descendants of its own

## Indications for use
Cutting and Dissecting Various Abdominal Tissue during Endoscopic (inclusive of laparoscopic) Surgical Procedures.

Source page: https://510kreport.com/device/K160706
Methodology: https://510kreport.com/methodology