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FDA 510(k)

FUNKY SUNGLASS

K-Number: K904981 · 1991-01-28

ApplicantMonogram International,Inc.
Decision Date1991-01-28
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FUNKY SUNGLASS is the device name listed in this FDA 510(k) record. The listed applicant is Monogram International,Inc.. It received FDA 510(k) clearance on 1991-01-28 under 510(k) number K904981. 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 FUNKY SUNGLASS?

FUNKY SUNGLASS is a medical device that received FDA 510(k) clearance on 1991-01-28. The listed applicant is Monogram International,Inc.. The 510(k) number is K904981.

When did FUNKY SUNGLASS receive FDA 510(k) clearance?

FUNKY SUNGLASS received FDA 510(k) clearance on 1991-01-28, under 510(k) number K904981.

Who is the listed applicant for FUNKY SUNGLASS?

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

What is the FDA product code for FUNKY SUNGLASS?

The FDA product code for FUNKY SUNGLASS 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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