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FDA 510(k)

SERIOUS SKINGLASSES

K-Number: K922120 · 1993-06-21

ApplicantSerious Skinglasses
Decision Date1993-06-21
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SERIOUS SKINGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Serious Skinglasses. It received FDA 510(k) clearance on 1993-06-21 under 510(k) number K922120. 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 SERIOUS SKINGLASSES?

SERIOUS SKINGLASSES is a medical device that received FDA 510(k) clearance on 1993-06-21. The listed applicant is Serious Skinglasses. The 510(k) number is K922120.

When did SERIOUS SKINGLASSES receive FDA 510(k) clearance?

SERIOUS SKINGLASSES received FDA 510(k) clearance on 1993-06-21, under 510(k) number K922120.

Who is the listed applicant for SERIOUS SKINGLASSES?

The FDA 510(k) record lists Serious Skinglasses as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERIOUS SKINGLASSES?

The FDA product code for SERIOUS SKINGLASSES 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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