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FDA 510(k)

TECHNA VISION AUTO-PERIMETER

K-Number: K853290 · 1985-11-12

ApplicantTechna Vision
Decision Date1985-11-12
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TECHNA VISION AUTO-PERIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Techna Vision. It received FDA 510(k) clearance on 1985-11-12 under 510(k) number K853290. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNA VISION AUTO-PERIMETER?

TECHNA VISION AUTO-PERIMETER is a medical device that received FDA 510(k) clearance on 1985-11-12. The listed applicant is Techna Vision. The 510(k) number is K853290.

When did TECHNA VISION AUTO-PERIMETER receive FDA 510(k) clearance?

TECHNA VISION AUTO-PERIMETER received FDA 510(k) clearance on 1985-11-12, under 510(k) number K853290.

Who is the listed applicant for TECHNA VISION AUTO-PERIMETER?

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 AUTO-PERIMETER?

The FDA product code for TECHNA VISION AUTO-PERIMETER is HPT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K862578TECHNA VISION CASTING RESINK853743TECHNA VISION, INC. ELECTRIC CHAIRK853744TECHNA VISION, INC.ELECTRIC TABLE

Related Devices (Code: HPT)

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.

K092187MAIA, MODEL 1Centervue S.P.A.K093213GUIDED PROGRESSION ANALYSIS ON THE HUMPHREY FIELD ANALYZER II AND II -I SERIESCarl Zeiss Meditec, Inc.K091579FORESEE HOMENotal Vision , Ltd.K063310TRUEFIELD ANALYZERSeeing Machines LimitedK050350THE NOTAL VISION PREVIEW PREFERENTIAL HYPERACUITY PERIMETER (PREVIEW PHP)Notal Vision, Inc.K023623NOVAVISION, MODEL 2.0Novavision, 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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