# K910132: Stryker Laparoscope

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Feb 21, 1991 after 43 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.
107 later devices descend from it; 3 cite it directly.
0 of 108 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
- K091515: Spy Scope Intra-Operative Operating System (2009), 106 descendants of its own
- K101077: DA Vinci Fluorescence Imaging Vision System, Model FF 100 (2011), 104 descendants of its own
- K124031: DA Vinci Fluorescence Imaging Vision System (2013), 103 descendants of its own
- K141077: DA Vinci Firefly Imaging System (2014), 87 descendants of its own
- K142310: Stryker Infrared Fluorescence (IRF) Imaging System (2014), 76 descendants of its own

Source page: https://510kreport.com/device/K910132
Methodology: https://510kreport.com/methodology