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FDA 510(k)

MARTIN SUNGLASSES

K-Number: K950456 · 1995-03-01

ApplicantJack Martin Co., Inc.
Decision Date1995-03-01
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MARTIN SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Jack Martin Co., Inc.. It received FDA 510(k) clearance on 1995-03-01 under 510(k) number K950456. 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 MARTIN SUNGLASSES?

MARTIN SUNGLASSES is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is Jack Martin Co., Inc.. The 510(k) number is K950456.

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

MARTIN SUNGLASSES received FDA 510(k) clearance on 1995-03-01, under 510(k) number K950456.

Who is the listed applicant for MARTIN SUNGLASSES?

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

What is the FDA product code for MARTIN SUNGLASSES?

The FDA product code for MARTIN SUNGLASSES is HQY.

Related Clinical Trials

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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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