# K010256: Ultravue/P 2000T, Ultravue/C 2000T (Hioxifilcon B) Soft (Multifocal Toric) Daily Wear Contact Lens (Clear & Blue Visibil

- Pathway: 510(k) (Traditional)
- Applicant: Opti-Centre Laboratories
- Decided: Mar 26, 2001 after 56 days
- Product code: LPL (Lenses, Soft Contact, Daily Wear)
- Device class: 2
- Regulation: 21 CFR 886.5925
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

Source page: https://510kreport.com/device/K010256
Methodology: https://510kreport.com/methodology