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FDA 510(k)

ULTRAVUE BLENDED BIFOCAL LENS

K-Number: K791721 · 1979-10-23

ApplicantAmerican Optical Corp.
Decision Date1979-10-23
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ULTRAVUE BLENDED BIFOCAL 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 1979-10-23 under 510(k) number K791721. 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 ULTRAVUE BLENDED BIFOCAL LENS?

ULTRAVUE BLENDED BIFOCAL LENS is a medical device that received FDA 510(k) clearance on 1979-10-23. The listed applicant is American Optical Corp.. The 510(k) number is K791721.

When did ULTRAVUE BLENDED BIFOCAL LENS receive FDA 510(k) clearance?

ULTRAVUE BLENDED BIFOCAL LENS received FDA 510(k) clearance on 1979-10-23, under 510(k) number K791721.

Who is the listed applicant for ULTRAVUE BLENDED BIFOCAL 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 ULTRAVUE BLENDED BIFOCAL LENS?

The FDA product code for ULTRAVUE BLENDED BIFOCAL LENS is HQG.

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Other records listing American Optical Corp. 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.

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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