# K870942: MVS Fiberoptic Lightpipe

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Surgical Products, Inc.
- Decided: Apr 3, 1987 after 25 days
- Product code: FST (Light, Surgical, Fiberoptic)
- Device class: 2
- Regulation: 21 CFR 878.4580
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 2 cite it directly.
0 of 10 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
- K982462: Fiber Optic Endoillumination Probe (1998), 7 descendants of its own
- K050807: 20G Sma Laser Fiber, Model LF100 (2005), 6 descendants of its own
- K121187: Katalyst Laser Probes, Katalyst Illuminated Laser Probes (2012), 5 descendants of its own
- K142830: Ophthalmed Bending Laser Probes (2015), 2 descendants of its own
- K191846: MAXReach Laser Probe (2019), 1 descendant of its own

Source page: https://510kreport.com/device/K870942
Methodology: https://510kreport.com/methodology