Cleared Traditional

K915266 - VISOR SUNGLASSES/LENS/NOVELTY VISOR

K915266 is an FDA 510(k) clearance for VISOR SUNGLASSES/LENS/NOVELTY VISOR, manufactured by Janlin Ent.. The device is a Class 1 Ophthalmic device with product code HQY cleared through the Traditional 510(k) pathway after a 287-day FDA review.

K915266 · Janlin Ent. · Ophthalmic device
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Sep 1992
Decision
287d
Days
Class 1
Risk

K915266 is an FDA 510(k) clearance for the VISOR SUNGLASSES/LENS/NOVELTY VISOR. Classified as Sunglasses (non-prescription Including Photosensitive) (product code HQY), Class I - General Controls.

Submitted by Janlin Ent. (Torrance, US). The FDA issued a Cleared decision on September 2, 1992 after a review of 287 days - an extended review cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5850 - 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 Janlin Ent. devices

FDA 510(k) Submission Details - K915266

510(k) Number K915266 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 20, 1991
Decision Date September 02, 1992
Days to Decision 287 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
177d slower than avg
Panel avg: 110d · This submission: 287d
Pathway characteristics
Predicate-based equivalence.

HQY Device Classification - Class 1, General Controls

Product Code HQY Sunglasses (non-prescription Including Photosensitive)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.5850
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - HQY Sunglasses (non-prescription Including Photosensitive)

All 124
Devices cleared under the same product code (HQY) and FDA review panel - the closest regulatory comparables to K915266.
SUNGLASSES WITH IMPACT RESISTANT LENSES
K955572 · Diamond Mark International Co., Ltd. · Jan 1996
UNISUN
K955539 · Steven Chen · Jan 1996
KMANZ II
K955611 · Gatorz LLC · Jan 1996
PHOTOCHROMIC LENS
K890725 · Ppg Industries, Inc. · Apr 1989
CALIUS-ISABEL CANOVAS SUNGLASSES
K890081 · Roseburg SA · Mar 1989
ASSENAT-BLESCHET SUNGLASSES
K885275 · Roseburg SA · Jan 1989