Cleared Traditional

K240477 - Saview SH 38 UV (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens (FDA 510(k) Clearance)

Also includes:
Saview SH 38 UV toric (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens Saview SH 38 UV multifocal (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens
Jul 2024
Decision
132d
Days
Class 2
Risk

K240477 is an FDA 510(k) clearance for the Saview SH 38 UV (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens. This device is classified as a Lenses, Soft Contact, Daily Wear (Class II - Special Controls, product code LPL).

Submitted by St. shine Optical Co., Ltd. (New Taipei City, TW). The FDA issued a Cleared decision on July 1, 2024, 132 days after receiving the submission on February 20, 2024.

This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.5925.

Submission Details

510(k) Number K240477 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 20, 2024
Decision Date July 01, 2024
Days to Decision 132 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF

Device Classification

Product Code LPL — Lenses, Soft Contact, Daily Wear
Device Class Class II - Special Controls
CFR Regulation 21 CFR 886.5925

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