# K080948: HD Endoeye Laparo-Thoraco Videoscope Olympus LTF Type VH

- Pathway: 510(k) (Traditional)
- Applicant: Olympus Medical Systems Corporation
- Decided: Sep 26, 2008 after 176 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.
54 later devices descend from it; 4 cite it directly.
0 of 55 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) LTF-V: named in the summary without a submission number

## Most influential descendants
- K111425: Olympus LTF-S190-10, Olumpus Otv-S190, Olympus CLV-S190 (2012), 34 descendants of its own
- K102379: LTF-Y0009; Maj-YOO41; Xoev-3D1 (2011), 33 descendants of its own
- K123365: Olympus LTF-190-10-3D, Maj-Y0154, Olympus CV-190 (2013), 19 descendants of its own
- K113203: Sony LMD-2451MT LCD Monitor (2012), 12 descendants of its own
- K111788: Endoeye HD II (2012), 10 descendants of its own

## Indications for use
This instrument has been designed to be used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the thoracic and abdominal cavities.

Source page: https://510kreport.com/device/K080948
Methodology: https://510kreport.com/methodology