SPECTACLE FRAME/EYEGLASS FRAME
K-Number: K935558 · 1994-01-25
Advertisement
Device Summary
Frequently Asked Questions
What is the SPECTACLE FRAME/EYEGLASS FRAME?
SPECTACLE FRAME/EYEGLASS FRAME is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Modern Optical , Ltd.. The 510(k) number is K935558.
When did SPECTACLE FRAME/EYEGLASS FRAME receive FDA 510(k) clearance?
SPECTACLE FRAME/EYEGLASS FRAME received FDA 510(k) clearance on 1994-01-25, under 510(k) number K935558.
Who is the listed applicant for SPECTACLE FRAME/EYEGLASS FRAME?
The FDA 510(k) record lists Modern Optical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPECTACLE FRAME/EYEGLASS FRAME?
The FDA product code for SPECTACLE FRAME/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.
Advertisement