# K961299: Precision UV (Vasurfilcon a)

- Pathway: 510(k) (Traditional)
- Applicant: Pilkington Barnes-Hind, Ltd.
- Decided: Oct 1, 1996 after 180 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
Longest line of descent: 1 generation back to K946012 (1995). 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)
- K946012: Precision UV (TM) (Vasurficon a), Pilkington Barnes-Hind, Ltd. (1995) Summary page 1.

## Most influential descendants
- K982988: Precision UV (Vasurfilcon a) (1999), 0 descendants of its own

## Indications for use
Precision UV™ (vasurfilcon A) Hydrophilic contact lenses are indicated for the correction of visual acuity in not-aphakic persons with non-diseased eyes that are myopic or hyperopic and may have 2.00 diopters (D) or less of corneal astigmatism that does not interfere with visual acuity. The contact lenses may be prescribed for daily wear as recommended by the eye care practitioner.

Source page: https://510kreport.com/device/K961299
Methodology: https://510kreport.com/methodology