EYEGLASS FRAME
K-Number: K926157 · 1993-05-06
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Device Summary
Frequently Asked Questions
What is the EYEGLASS FRAME?
EYEGLASS FRAME is a medical device that received FDA 510(k) clearance on 1993-05-06. The listed applicant is Roi Factory Direct Frame Co.. The 510(k) number is K926157.
When did EYEGLASS FRAME receive FDA 510(k) clearance?
EYEGLASS FRAME received FDA 510(k) clearance on 1993-05-06, under 510(k) number K926157.
Who is the listed applicant for EYEGLASS FRAME?
The FDA 510(k) record lists Roi Factory Direct Frame Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EYEGLASS FRAME?
The FDA product code for 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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