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FDA 510(k)

BLENDED BIFOCAL

K-Number: K802749 · 1980-12-17

ApplicantRobinson-Houchin, Inc.
Decision Date1980-12-17
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BLENDED BIFOCAL is the device name listed in this FDA 510(k) record. The listed applicant is Robinson-Houchin, Inc.. It received FDA 510(k) clearance on 1980-12-17 under 510(k) number K802749. 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 BLENDED BIFOCAL?

BLENDED BIFOCAL is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Robinson-Houchin, Inc.. The 510(k) number is K802749.

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

BLENDED BIFOCAL received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802749.

Who is the listed applicant for BLENDED BIFOCAL?

The FDA 510(k) record lists Robinson-Houchin, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLENDED BIFOCAL?

The FDA product code for BLENDED BIFOCAL 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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