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FDA 510(k)

FESAN SUNGLASSES

K-Number: K902117 · 1990-07-24

ApplicantFesan, S.A.
Decision Date1990-07-24
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FESAN SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Fesan, S.A.. It received FDA 510(k) clearance on 1990-07-24 under 510(k) number K902117. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FESAN SUNGLASSES?

FESAN SUNGLASSES is a medical device that received FDA 510(k) clearance on 1990-07-24. The listed applicant is Fesan, S.A.. The 510(k) number is K902117.

When did FESAN SUNGLASSES receive FDA 510(k) clearance?

FESAN SUNGLASSES received FDA 510(k) clearance on 1990-07-24, under 510(k) number K902117.

Who is the listed applicant for FESAN SUNGLASSES?

The FDA 510(k) record lists Fesan, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FESAN SUNGLASSES?

The FDA product code for FESAN SUNGLASSES is HQY.

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Related Devices (Code: HQY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K974852NON-PRESCRIPTION SUNGLASSESChia Hui Spectacles Mfg. Corp.K974860NON-PRESCRIPTION SUNGLASSESWenzhou Ming Ming Optical Co. , Ltd.K974861NON-PRESCRIPTION SUNGLASSESWenzhou Hindar Optical Co., Ltd.K974511SUNGLASSESSun World Intl., Inc.K974441SUNGLASSESHip Shing Fat Co., Ltd.K973528SUNGLASSESJeou Jeou Long Industrial Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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