# K051104: Eye See Multipurpose, NO-Rub Contact Lens Solution

- Pathway: 510(k) (Traditional)
- Applicant: Lapis Lazuli, NV
- Decided: May 31, 2006 after 394 days
- Product code: LPN (Accessories, Soft Lens Products)
- Device class: 2
- Regulation: 21 CFR 886.5928
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K030092 (2003). 1 ancestor in all.
1 later device descends 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)
- K030092: Complete Brand Multi-Purpose Solution, Advanced Medical Optics, Inc. (2003) Summary page 3.

## Cited in the summary but kept off the family tree
- K033854: NRC07 Multi-purpose solution. Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree Summary page 3.

## Most influential descendants
- K070767: Eye See Multipurpose Contact Lens Solution (2007), 0 descendants of its own

## Indications for use
EYE SEETM Multipurpose Contact Lens Solution is indicated for use in the daily cleaning, removal of protein deposits, rinsing, chemical (not heat) disinfection, and storage of soft (hydrophilic) contact lenses, as recommended by your eye care practitioner.

Source page: https://510kreport.com/device/K051104
Methodology: https://510kreport.com/methodology