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FDA 510(k)

SUNGLASES

K-Number: K851163 · 1985-05-30

ApplicantFull See Glasses Ind. Co., Ltd.
Decision Date1985-05-30
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNGLASES is the device name listed in this FDA 510(k) record. The listed applicant is Full See Glasses Ind. Co., Ltd.. It received FDA 510(k) clearance on 1985-05-30 under 510(k) number K851163. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNGLASES?

SUNGLASES is a medical device that received FDA 510(k) clearance on 1985-05-30. The listed applicant is Full See Glasses Ind. Co., Ltd.. The 510(k) number is K851163.

When did SUNGLASES receive FDA 510(k) clearance?

SUNGLASES received FDA 510(k) clearance on 1985-05-30, under 510(k) number K851163.

Who is the listed applicant for SUNGLASES?

The FDA 510(k) record lists Full See Glasses Ind. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNGLASES?

The FDA product code for SUNGLASES is HQG.

Related Clinical Trials

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Related Devices (Code: HQG)

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.

K935919SUNGLASSESJa-Ru, Inc.K9207950R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEXOptical Radiation Corp.K900091MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOROnufryk Low Vision Ent.K884360SEIKO P-6 PROGRESSIVE SPECTACLE LENSESSeiko Corp.K882814NEOLENS PRESCRIPTION SPECTACLE LENSNeolens, Inc.K882308CR-39 PLASTIC LENSES FOR EYEGLASSESAutomated Lens System

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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