# K980079: Coherent Tissue Morcellator Kit and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Lumenis, Inc.
- Decided: Apr 9, 1998 after 90 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 K910939 (1991). 3 ancestors in all.
8 later devices descend from it; 1 cites it directly.
1 of 12 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K925851: Cook Tissue Morcellator, Cook Urological, Inc. (1993) Summary page 1.
- K910939: Cook Tissue Morcellator, Cook Urological, Inc. (1991) Summary page 1.
- K935604: Lasersonics Tissue Morcellator Set, Heraeus Surgical, Inc. (1994) Summary page 1.

## Most influential descendants
- K050639: Lumenis Versacut Tissue Morcellator System (2005), 7 descendants of its own
- K133272: Versacut + Tissue Morcellator (2014), 5 descendants of its own
- K192499: Cyber Blade (2020), 2 descendants of its own
- K213597: MultiCut Solo (2023), 1 descendant of its own
- K260884: UNIDRIVE Select System (2026), 0 descendants of its own

## Indications for use
The Coherent Tissue Morcellator Kit is intended for use under direct or endoscopic visualization for the morcellation and removal of dissected tissue during pelviscopic, laparoscopic, percutaneous, and open surgical procedures whenever access to the surgical site is limited.

Source page: https://510kreport.com/device/K980079
Methodology: https://510kreport.com/methodology