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FDA 510(k)

PHOTOLITE AOLITE TINTOMATIC LENS

K-Number: K812051 · 1981-09-08

ApplicantAmerican Optical Corp.
Decision Date1981-09-08
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHOTOLITE AOLITE TINTOMATIC LENS is the device name listed in this FDA 510(k) record. The listed applicant is American Optical Corp.. It received FDA 510(k) clearance on 1981-09-08 under 510(k) number K812051. 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 PHOTOLITE AOLITE TINTOMATIC LENS?

PHOTOLITE AOLITE TINTOMATIC LENS is a medical device that received FDA 510(k) clearance on 1981-09-08. The listed applicant is American Optical Corp.. The 510(k) number is K812051.

When did PHOTOLITE AOLITE TINTOMATIC LENS receive FDA 510(k) clearance?

PHOTOLITE AOLITE TINTOMATIC LENS received FDA 510(k) clearance on 1981-09-08, under 510(k) number K812051.

Who is the listed applicant for PHOTOLITE AOLITE TINTOMATIC LENS?

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

What is the FDA product code for PHOTOLITE AOLITE TINTOMATIC LENS?

The FDA product code for PHOTOLITE AOLITE TINTOMATIC LENS is HQG.

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Other records listing American Optical Corp. as applicant

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K950881PHACO TIPK950880AOI UNIVERSAL ULTRASONIC HANDPIECEK931354P4000 PHACOEMULSIFIERK931358AORP4000 REUSABLE PAKK931357AOD4000 DISPOSABLE PAKK820790FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3

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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

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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