# K982515: Power-Drive, Wisap Model #7688PD/7688PD1

- Pathway: 510(k) (Traditional)
- Applicant: Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh
- Decided: Jan 19, 1999 after 183 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K080365: Morce Power Plus and Variocarve Morcellator (2009), 0 descendants of its own

## Indications for use
This device is restricted to use by authorized expert personnel /physicians. The WISAP POWER-DRIVE is a laparoscopic accessory to be used in connection ith the S*EXM*M*-Set. ' _ ‘;t allows cutting of tissue cylinders out 9f myoma and uteri by continuous rotation of ‘the motor drive or additional intermittent mar-lual rotation. The POWER-DRIVE may only be used for horizontal morcellation.

Source page: https://510kreport.com/device/K982515
Methodology: https://510kreport.com/methodology