# K955456: Oes Laparo-Thoraco Videoscope (Rigid)

- Pathway: 510(k) (Traditional)
- Applicant: Olympus America, Inc.
- Decided: Feb 22, 1996 after 85 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.
12 later devices descend from it; 2 cite it directly.
0 of 13 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
- K111788: Endoeye HD II (2012), 10 descendants of its own
- K190744: Endoeye HD II (WA50040A, WA50042A, WA50050A, WA50052A) (2019), 6 descendants of its own
- K193026: Visera Elite II Video System Center, Visera Elite II Endoeye 3D (2020), 5 descendants of its own
- K201200: Visera Elite II Video System Center (2020), 4 descendants of its own
- K242067: Visera Elite Iii Video System Center Olympus Otv-S700; Visera Elite Iii Led Light Source Olympus CLL-S700; 4K Camera Head Olympus CH-S700-XZ-EA (2025), 2 descendants of its own

Source page: https://510kreport.com/device/K955456
Methodology: https://510kreport.com/methodology