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FDA 510(k)

MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR

K-Number: K900091 · 1990-04-04

ApplicantOnufryk Low Vision Ent.
Decision Date1990-04-04
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Onufryk Low Vision Ent.. It received FDA 510(k) clearance on 1990-04-04 under 510(k) number K900091. 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 MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR?

MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR is a medical device that received FDA 510(k) clearance on 1990-04-04. The listed applicant is Onufryk Low Vision Ent.. The 510(k) number is K900091.

When did MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR receive FDA 510(k) clearance?

MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR received FDA 510(k) clearance on 1990-04-04, under 510(k) number K900091.

Who is the listed applicant for MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR?

The FDA 510(k) record lists Onufryk Low Vision Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR?

The FDA product code for MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR 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.K884360SEIKO P-6 PROGRESSIVE SPECTACLE LENSESSeiko Corp.K882814NEOLENS PRESCRIPTION SPECTACLE LENSNeolens, Inc.K882308CR-39 PLASTIC LENSES FOR EYEGLASSESAutomated Lens SystemK881225OPHTHALMIC SPECTACLE LENS BLANKSBeta Optical Co, Inc.

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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