Cleared Traditional

K973528 - SUNGLASSES
(FDA 510(k) Clearance)

Dec 1997
Decision
82d
Days
Class 1
Risk

K973528 is an FDA 510(k) clearance for the SUNGLASSES. This device is classified as a Sunglasses (non-prescription Including Photosensitive) (Class I - General Controls, product code HQY).

Submitted by Jeou Jeou Long Industrial Co., Ltd. (Kaohsiung, TW). The FDA issued a Cleared decision on December 8, 1997, 82 days after receiving the submission on September 17, 1997.

This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.5850.

Submission Details

510(k) Number K973528 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 17, 1997
Decision Date December 08, 1997
Days to Decision 82 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement

Device Classification

Product Code HQY — Sunglasses (non-prescription Including Photosensitive)
Device Class Class I - General Controls
CFR Regulation 21 CFR 886.5850

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