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FDA 510(k)

TECHNA VISION CASTING RESIN

K-Number: K862578 · 1986-07-23

ApplicantTechna Vision
Decision Date1986-07-23
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TECHNA VISION CASTING RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Techna Vision. It received FDA 510(k) clearance on 1986-07-23 under 510(k) number K862578. 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 TECHNA VISION CASTING RESIN?

TECHNA VISION CASTING RESIN is a medical device that received FDA 510(k) clearance on 1986-07-23. The listed applicant is Techna Vision. The 510(k) number is K862578.

When did TECHNA VISION CASTING RESIN receive FDA 510(k) clearance?

TECHNA VISION CASTING RESIN received FDA 510(k) clearance on 1986-07-23, under 510(k) number K862578.

Who is the listed applicant for TECHNA VISION CASTING RESIN?

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

What is the FDA product code for TECHNA VISION CASTING RESIN?

The FDA product code for TECHNA VISION CASTING RESIN is HQG.

Related Clinical Trials

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.

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Other records listing Techna Vision 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.

K853290TECHNA VISION AUTO-PERIMETERK853743TECHNA VISION, INC. ELECTRIC CHAIRK853744TECHNA VISION, INC.ELECTRIC TABLE

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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