Cleared Traditional

K961299 - PRECISION UV (VASURFILCON A)

K961299 is an FDA 510(k) clearance for PRECISION UV (VASURFILCON A), manufactured by Pilkington Barnes-Hind, Ltd.. The device is a Class 2 Ophthalmic device with product code LPL cleared through the Traditional 510(k) pathway after a 180-day FDA review.

K961299 · Pilkington Barnes-Hind, Ltd. · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1996
Decision
180d
Days
Class 2
Risk

K961299 is an FDA 510(k) clearance for the PRECISION UV (VASURFILCON A). Classified as Lenses, Soft Contact, Daily Wear (product code LPL), Class II - Special Controls.

Submitted by Pilkington Barnes-Hind, Ltd. (Sunnyvale, US). The FDA issued a Cleared decision on October 1, 1996 after a review of 180 days - an extended review cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5925 - the FDA ophthalmic device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Ophthalmic review framework, consistent with the majority of Class II 510(k) submissions.

View all Pilkington Barnes-Hind, Ltd. devices

FDA 510(k) Submission Details - K961299

510(k) Number K961299 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 04, 1996
Decision Date October 01, 1996
Days to Decision 180 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
70d slower than avg
Panel avg: 110d · This submission: 180d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LPL Device Classification - Class 2, Special Controls

Product Code LPL Lenses, Soft Contact, Daily Wear
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.5925
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Ophthalmic devices follow this clearance model.

Regulatory Peers - LPL Lenses, Soft Contact, Daily Wear

All 350
Devices cleared under the same product code (LPL) and FDA review panel - the closest regulatory comparables to K961299.
DAILIES (NELFILCON A) ONE-DAY SOFT CONTACT LENS
K963487 · Ciba Vision Corporation · Nov 1996
METRO FOCAL ASPHERIC (POLYMACON)
K961606 · Metro Optics of Austin, Inc. · Nov 1996
SPECIALTY PROGRESSIVE(METHAFILCON A)MULTIFOCAL SOFT(HYDROPHILIC)CONTACT LENS FOR DAILY WEAR(CLEAR AND TINTED)
K963488 · Specialty Ultravision, Inc. · Nov 1996
FLEXLENS
K961943 · Flexlens, Inc. · Oct 1996
FLEXLENS(METHAFILCON A)
K962000 · Flexlens, Inc. · Oct 1996
ACUVUE (ETAFILCON A) CONTACT LENS CLEAR & W/VISIBILITY TINT W/UV BLOCKER
K962804 · Vistakon, Johnson & Johnson Vision Products, Inc. · Oct 1996