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FDA 510(k)

SPECTACLE SUNGLASSES (NON-PERSCRIPTION)

K-Number: K934034 · 1993-10-18

ApplicantH.M.O. Optical, Inc.
Decision Date1993-10-18
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE SUNGLASSES (NON-PERSCRIPTION) is the device name listed in this FDA 510(k) record. The listed applicant is H.M.O. Optical, Inc.. It received FDA 510(k) clearance on 1993-10-18 under 510(k) number K934034. 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 SUNGLASSES (NON-PERSCRIPTION)?

SPECTACLE SUNGLASSES (NON-PERSCRIPTION) is a medical device that received FDA 510(k) clearance on 1993-10-18. The listed applicant is H.M.O. Optical, Inc.. The 510(k) number is K934034.

When did SPECTACLE SUNGLASSES (NON-PERSCRIPTION) receive FDA 510(k) clearance?

SPECTACLE SUNGLASSES (NON-PERSCRIPTION) received FDA 510(k) clearance on 1993-10-18, under 510(k) number K934034.

Who is the listed applicant for SPECTACLE SUNGLASSES (NON-PERSCRIPTION)?

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

What is the FDA product code for SPECTACLE SUNGLASSES (NON-PERSCRIPTION)?

The FDA product code for SPECTACLE SUNGLASSES (NON-PERSCRIPTION) 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing H.M.O. Optical, Inc. as applicant

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.

K934033SPECTACLE FRAMES

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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