# K003252: Complete Brand Multi-Purpose Solution

- Pathway: 510(k) (Traditional)
- Applicant: Allergan, Inc.
- Decided: Feb 21, 2001 after 127 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
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
- K014202: Complete Brand Multi-Purpose Solution (2002), 1 descendant of its own
- K202932: ABT12 multi-purpose solution (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K003252
Methodology: https://510kreport.com/methodology