# K854507: Storz MVS 19 & 20 Gauge Scleral Plugs

- Pathway: 510(k) (Traditional)
- Applicant: Storz Instrument Co.
- Decided: Feb 7, 1986 after 87 days
- Product code: LXP (Plug, Scleral)
- Device class: 2
- Regulation: 21 CFR 886.4155
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K022186: Scleral Plugs, 19 and 20 Gauge (2003), 0 descendants of its own
- K990872: Scleral Plugs, 19 and 20 Gauge (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K854507
Methodology: https://510kreport.com/methodology