# K854587: Storz MVS Disposable Fiberoptic Lightpipe

- Pathway: 510(k) (Traditional)
- Applicant: Storz Instrument Co.
- Decided: Feb 4, 1986 after 78 days
- Product code: HBI (Illuminator, Fiberoptic, Surgical Field)
- 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K961036: Mbi Fiberoptic Endo-Illuminator (1996), 2 descendants of its own
- K964553: Mbi CO-Axial Illuminated Retinal Pick (1997), 0 descendants of its own
- K964405: Mbi Illuminated Retinal Pick (1997), 0 descendants of its own
- K960007: Storz MVS 1011A Disposable Fiberoptic Endoilluminator (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K854587
Methodology: https://510kreport.com/methodology