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FDA 510(k)

TECHNA VISION, INC. ELECTRIC CHAIR

K-Number: K853743 · 1985-10-17

ApplicantTechna Vision
Decision Date1985-10-17
Product CodeHME
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TECHNA VISION, INC. ELECTRIC CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Techna Vision. It received FDA 510(k) clearance on 1985-10-17 under 510(k) number K853743. The device is classified under product code HME. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNA VISION, INC. ELECTRIC CHAIR?

TECHNA VISION, INC. ELECTRIC CHAIR is a medical device that received FDA 510(k) clearance on 1985-10-17. The listed applicant is Techna Vision. The 510(k) number is K853743.

When did TECHNA VISION, INC. ELECTRIC CHAIR receive FDA 510(k) clearance?

TECHNA VISION, INC. ELECTRIC CHAIR received FDA 510(k) clearance on 1985-10-17, under 510(k) number K853743.

Who is the listed applicant for TECHNA VISION, INC. ELECTRIC CHAIR?

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, INC. ELECTRIC CHAIR?

The FDA product code for TECHNA VISION, INC. ELECTRIC CHAIR is HME.

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.

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.

Related Devices (Code: HME)

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.

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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