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FDA 510(k)

CARTIER SUNGLASSES, MUST DE

K-Number: K900907 · 1990-09-19

ApplicantCartier, Inc.
Decision Date1990-09-19
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CARTIER SUNGLASSES, MUST DE is the device name listed in this FDA 510(k) record. The listed applicant is Cartier, Inc.. It received FDA 510(k) clearance on 1990-09-19 under 510(k) number K900907. 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 CARTIER SUNGLASSES, MUST DE?

CARTIER SUNGLASSES, MUST DE is a medical device that received FDA 510(k) clearance on 1990-09-19. The listed applicant is Cartier, Inc.. The 510(k) number is K900907.

When did CARTIER SUNGLASSES, MUST DE receive FDA 510(k) clearance?

CARTIER SUNGLASSES, MUST DE received FDA 510(k) clearance on 1990-09-19, under 510(k) number K900907.

Who is the listed applicant for CARTIER SUNGLASSES, MUST DE?

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

What is the FDA product code for CARTIER SUNGLASSES, MUST DE?

The FDA product code for CARTIER SUNGLASSES, MUST DE 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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