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FDA 510(k)

ULTRAVIOLET LIGHT PROTECTVE EYEWERE

K-Number: K880666 · 1988-06-28

Decision Date1988-06-28
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ULTRAVIOLET LIGHT PROTECTVE EYEWERE is the device name listed in this FDA 510(k) record. The listed applicant is Free Sun Intl. AB. It received FDA 510(k) clearance on 1988-06-28 under 510(k) number K880666. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAVIOLET LIGHT PROTECTVE EYEWERE?

ULTRAVIOLET LIGHT PROTECTVE EYEWERE is a medical device that received FDA 510(k) clearance on 1988-06-28. The listed applicant is Free Sun Intl. AB. The 510(k) number is K880666.

When did ULTRAVIOLET LIGHT PROTECTVE EYEWERE receive FDA 510(k) clearance?

ULTRAVIOLET LIGHT PROTECTVE EYEWERE received FDA 510(k) clearance on 1988-06-28, under 510(k) number K880666.

Who is the listed applicant for ULTRAVIOLET LIGHT PROTECTVE EYEWERE?

The FDA 510(k) record lists Free Sun Intl. AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRAVIOLET LIGHT PROTECTVE EYEWERE?

The FDA product code for ULTRAVIOLET LIGHT PROTECTVE EYEWERE is HOY.

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: HOY)

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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