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FDA 510(k)

RUBBER FRAME SUNGLASSES

K-Number: K922508 · 1992-08-26

ApplicantJedda Dist., Inc.
Decision Date1992-08-26
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RUBBER FRAME SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Jedda Dist., Inc.. It received FDA 510(k) clearance on 1992-08-26 under 510(k) number K922508. 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 RUBBER FRAME SUNGLASSES?

RUBBER FRAME SUNGLASSES is a medical device that received FDA 510(k) clearance on 1992-08-26. The listed applicant is Jedda Dist., Inc.. The 510(k) number is K922508.

When did RUBBER FRAME SUNGLASSES receive FDA 510(k) clearance?

RUBBER FRAME SUNGLASSES received FDA 510(k) clearance on 1992-08-26, under 510(k) number K922508.

Who is the listed applicant for RUBBER FRAME SUNGLASSES?

The FDA 510(k) record lists Jedda Dist., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RUBBER FRAME SUNGLASSES?

The FDA product code for RUBBER FRAME 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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