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FDA 510(k)

OCCU-TECH VISION TEST

K-Number: K881971 · 1988-11-25

Decision Date1988-11-25
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OCCU-TECH VISION TEST is the device name listed in this FDA 510(k) record. The listed applicant is Applied Vision Concepts, Inc.. It received FDA 510(k) clearance on 1988-11-25 under 510(k) number K881971. 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 OCCU-TECH VISION TEST?

OCCU-TECH VISION TEST is a medical device that received FDA 510(k) clearance on 1988-11-25. The listed applicant is Applied Vision Concepts, Inc.. The 510(k) number is K881971.

When did OCCU-TECH VISION TEST receive FDA 510(k) clearance?

OCCU-TECH VISION TEST received FDA 510(k) clearance on 1988-11-25, under 510(k) number K881971.

Who is the listed applicant for OCCU-TECH VISION TEST?

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

What is the FDA product code for OCCU-TECH VISION TEST?

The FDA product code for OCCU-TECH VISION TEST is HOX.

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.

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.

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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