# K935604: Lasersonics Tissue Morcellator Set

- Pathway: 510(k) (Traditional)
- Applicant: Heraeus Surgical, Inc.
- Decided: Mar 23, 1994 after 124 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
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
1 of 10 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K980079: Coherent Tissue Morcellator Kit and Accessories (1998), 8 descendants of its own
- 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

Source page: https://510kreport.com/device/K935604
Methodology: https://510kreport.com/methodology