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FDA 510(k)

SPECTACLE PRESCRIPTION LENSES

K-Number: K853110 · 1985-08-09

ApplicantAncie Laboratories
Decision Date1985-08-09
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE PRESCRIPTION LENSES is the device name listed in this FDA 510(k) record. The listed applicant is Ancie Laboratories. It received FDA 510(k) clearance on 1985-08-09 under 510(k) number K853110. 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 SPECTACLE PRESCRIPTION LENSES?

SPECTACLE PRESCRIPTION LENSES is a medical device that received FDA 510(k) clearance on 1985-08-09. The listed applicant is Ancie Laboratories. The 510(k) number is K853110.

When did SPECTACLE PRESCRIPTION LENSES receive FDA 510(k) clearance?

SPECTACLE PRESCRIPTION LENSES received FDA 510(k) clearance on 1985-08-09, under 510(k) number K853110.

Who is the listed applicant for SPECTACLE PRESCRIPTION LENSES?

The FDA 510(k) record lists Ancie Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTACLE PRESCRIPTION LENSES?

The FDA product code for SPECTACLE PRESCRIPTION LENSES is HQG.

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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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