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FDA 510(k)

MULTIPLE SPECTACLE LENS

K-Number: K871961 · 1987-06-03

ApplicantKorea Asahi Optical Co., Ltd.
Decision Date1987-06-03
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULTIPLE SPECTACLE LENS is the device name listed in this FDA 510(k) record. The listed applicant is Korea Asahi Optical Co., Ltd.. It received FDA 510(k) clearance on 1987-06-03 under 510(k) number K871961. 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 MULTIPLE SPECTACLE LENS?

MULTIPLE SPECTACLE LENS is a medical device that received FDA 510(k) clearance on 1987-06-03. The listed applicant is Korea Asahi Optical Co., Ltd.. The 510(k) number is K871961.

When did MULTIPLE SPECTACLE LENS receive FDA 510(k) clearance?

MULTIPLE SPECTACLE LENS received FDA 510(k) clearance on 1987-06-03, under 510(k) number K871961.

Who is the listed applicant for MULTIPLE SPECTACLE LENS?

The FDA 510(k) record lists Korea Asahi Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPLE SPECTACLE LENS?

The FDA product code for MULTIPLE SPECTACLE LENS is HQG.

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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Other records listing Korea Asahi Optical Co., Ltd. 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.

K871649CLASSIC 70 LENS

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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