OPTICAL OR EYEGLASS FRAME
K-Number: K883226 · 1988-08-24
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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