# K942201: Laparoscopy Dilation System

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: May 25, 1994 after 20 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.
11 later devices descend from it; 3 cite it directly.
0 of 12 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
- K970105: Riwo Cut-Morcellator Existing of Knife/Cutting Sleeve/Protection Sleeve/Claw Grasping Forceps (1997), 7 descendants of its own
- K041610: Morce Scope Set 8970 with Power Control 2303 and Suction Pump 2207 (2004), 6 descendants of its own
- K192499: Cyber Blade (2020), 2 descendants of its own
- K213597: MultiCut Solo (2023), 1 descendant of its own
- K041321: Veroscope Optical Veress Cannula & Dilation Tube System (2004), 1 descendant of its own

Source page: https://510kreport.com/device/K942201
Methodology: https://510kreport.com/methodology