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FDA 510(k)

TESTING VISUAL ACUITY

K-Number: K833778 · 1984-01-04

ApplicantTechnical Enginuities Co.
Decision Date1984-01-04
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TESTING VISUAL ACUITY is the device name listed in this FDA 510(k) record. The listed applicant is Technical Enginuities Co.. It received FDA 510(k) clearance on 1984-01-04 under 510(k) number K833778. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TESTING VISUAL ACUITY?

TESTING VISUAL ACUITY is a medical device that received FDA 510(k) clearance on 1984-01-04. The listed applicant is Technical Enginuities Co.. The 510(k) number is K833778.

When did TESTING VISUAL ACUITY receive FDA 510(k) clearance?

TESTING VISUAL ACUITY received FDA 510(k) clearance on 1984-01-04, under 510(k) number K833778.

Who is the listed applicant for TESTING VISUAL ACUITY?

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

What is the FDA product code for TESTING VISUAL ACUITY?

The FDA product code for TESTING VISUAL ACUITY is HOX.

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Related Devices (Code: HOX)

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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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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