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FDA 510(k)

SUNGLASSES TOKYO BAY

K-Number: K942500 · 1994-07-12

ApplicantTokyo Bay, Inc.
Decision Date1994-07-12
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNGLASSES TOKYO BAY is the device name listed in this FDA 510(k) record. The listed applicant is Tokyo Bay, Inc.. It received FDA 510(k) clearance on 1994-07-12 under 510(k) number K942500. 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 SUNGLASSES TOKYO BAY?

SUNGLASSES TOKYO BAY is a medical device that received FDA 510(k) clearance on 1994-07-12. The listed applicant is Tokyo Bay, Inc.. The 510(k) number is K942500.

When did SUNGLASSES TOKYO BAY receive FDA 510(k) clearance?

SUNGLASSES TOKYO BAY received FDA 510(k) clearance on 1994-07-12, under 510(k) number K942500.

Who is the listed applicant for SUNGLASSES TOKYO BAY?

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

What is the FDA product code for SUNGLASSES TOKYO BAY?

The FDA product code for SUNGLASSES TOKYO BAY is HQY.

Related Clinical Trials

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.

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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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