# K001666: Modification to Intuitive Surgical Stereo View Endoscopic System

- Pathway: 510(k) (Traditional)
- Applicant: Intuitive Surgical, Inc.
- Decided: Aug 24, 2000 after 85 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.
5 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have 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
- K080155: Modification to:Intuitive Surgical Stereo View Endoscopic System (2008), 3 descendants of its own
- K191043: da Vinci Handheld Camera (2019), 1 descendant of its own
- K241913: da Vinci Handheld Camera (2024), 0 descendants of its own
- K170641: da Vinci S/Si Endoscopes, da Vinci Xi Endoscopes (2017), 0 descendants of its own
- K013952: Intuitive Surgical Stero View Endoscopic System (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K001666
Methodology: https://510kreport.com/methodology
