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FDA 510(k)

SPECTACLE, FRAME AND SUNGLASSES

K-Number: K881278 · 1988-05-25

ApplicantNouvelle Ligne Paris
Decision Date1988-05-25
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE, FRAME AND SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Nouvelle Ligne Paris. It received FDA 510(k) clearance on 1988-05-25 under 510(k) number K881278. 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 SPECTACLE, FRAME AND SUNGLASSES?

SPECTACLE, FRAME AND SUNGLASSES is a medical device that received FDA 510(k) clearance on 1988-05-25. The listed applicant is Nouvelle Ligne Paris. The 510(k) number is K881278.

When did SPECTACLE, FRAME AND SUNGLASSES receive FDA 510(k) clearance?

SPECTACLE, FRAME AND SUNGLASSES received FDA 510(k) clearance on 1988-05-25, under 510(k) number K881278.

Who is the listed applicant for SPECTACLE, FRAME AND SUNGLASSES?

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

What is the FDA product code for SPECTACLE, FRAME AND SUNGLASSES?

The FDA product code for SPECTACLE, FRAME AND 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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