# K213597: MultiCut Solo

- Pathway: 510(k) (Traditional)
- Applicant: Asclepion Laser Technologies GmbH
- Decided: Jan 18, 2023 after 432 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: 5 generations back to K871250 (1987). 17 ancestors in all.
1 later device descends from it; 1 cites it directly.
1 of 19 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133272: Versacut + Tissue Morcellator, Lumenis, Ltd. (2014) Summary page 4.
- K041610: Morce Scope Set 8970 with Power Control 2303 and Suction Pump 2207, Richard Wolf Medical Instruments Corp. (2004) Summary page 4.

## Most influential descendants
- K240831: MultiCut Solo (2024), 0 descendants of its own

## Indications for use
The MultiCut Solo Morcellator is intended for use under endoscopic visualization for the transurethral mechanical morcellation and removal of the adenoma after enucleation of the prostate during endoscopic surgical procedures in urology.

Source page: https://510kreport.com/device/K213597
Methodology: https://510kreport.com/methodology