# K841599: Storz Universal Eye Shield

- Pathway: 510(k) (Traditional)
- Applicant: Storz Instrument Co.
- Decided: May 22, 1984 after 34 days
- Product code: HOY (Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear))
- Device class: 1
- Regulation: 21 CFR 886.4750
- 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; 1 cites 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
- K012530: AA-1 System (2001), 1 descendant of its own
- K023623: Novavision, Model 2.0 (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K841599
Methodology: https://510kreport.com/methodology