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FDA 510(k)

OPTICAL OR EYEGLASS FRAME

K-Number: K883226 · 1988-08-24

Decision Date1988-08-24
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTICAL OR EYEGLASS FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Unique Optic , Ltd.. It received FDA 510(k) clearance on 1988-08-24 under 510(k) number K883226. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTICAL OR EYEGLASS FRAME?

OPTICAL OR EYEGLASS FRAME is a medical device that received FDA 510(k) clearance on 1988-08-24. The listed applicant is Unique Optic , Ltd.. The 510(k) number is K883226.

When did OPTICAL OR EYEGLASS FRAME receive FDA 510(k) clearance?

OPTICAL OR EYEGLASS FRAME received FDA 510(k) clearance on 1988-08-24, under 510(k) number K883226.

Who is the listed applicant for OPTICAL OR EYEGLASS FRAME?

The FDA 510(k) record lists Unique Optic , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPTICAL OR EYEGLASS FRAME?

The FDA product code for OPTICAL OR EYEGLASS FRAME is HQZ.

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: HQZ)

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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