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FDA 510(k)

NON PRESCRIPTION SUN GLASSES

K-Number: K960650 · 1996-03-19

ApplicantSolovision Optical, Inc.
Decision Date1996-03-19
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NON PRESCRIPTION SUN GLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Solovision Optical, Inc.. It received FDA 510(k) clearance on 1996-03-19 under 510(k) number K960650. 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 NON PRESCRIPTION SUN GLASSES?

NON PRESCRIPTION SUN GLASSES is a medical device that received FDA 510(k) clearance on 1996-03-19. The listed applicant is Solovision Optical, Inc.. The 510(k) number is K960650.

When did NON PRESCRIPTION SUN GLASSES receive FDA 510(k) clearance?

NON PRESCRIPTION SUN GLASSES received FDA 510(k) clearance on 1996-03-19, under 510(k) number K960650.

Who is the listed applicant for NON PRESCRIPTION SUN GLASSES?

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

What is the FDA product code for NON PRESCRIPTION SUN GLASSES?

The FDA product code for NON PRESCRIPTION SUN GLASSES 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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