# K960640: S*E*M*M* Set for Moto Drive Wisap #7689 SSM (Modification)

- Pathway: 510(k) (Traditional)
- Applicant: Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh
- Decided: Feb 14, 1997 after 368 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 3 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K101458: Lina Xcise Model  Mor-1515 (2011), 1 descendant of its own
- K243821: i-Cut (2025), 0 descendants of its own
- K091010: Trokamed Morcellator (2011), 0 descendants of its own
- K080365: Morce Power Plus and Variocarve Morcellator (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K960640
Methodology: https://510kreport.com/methodology