SPECTACLE FRAME OR EYEGLASS FRAMES
K-Number: K945176 · 1994-12-15
Advertisement
Device Summary
Frequently Asked Questions
What is the SPECTACLE FRAME OR EYEGLASS FRAMES?
SPECTACLE FRAME OR EYEGLASS FRAMES is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Optipia Trading Co.. The 510(k) number is K945176.
When did SPECTACLE FRAME OR EYEGLASS FRAMES receive FDA 510(k) clearance?
SPECTACLE FRAME OR EYEGLASS FRAMES received FDA 510(k) clearance on 1994-12-15, under 510(k) number K945176.
Who is the listed applicant for SPECTACLE FRAME OR EYEGLASS FRAMES?
The FDA 510(k) record lists Optipia Trading Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPECTACLE FRAME OR EYEGLASS FRAMES?
The FDA product code for SPECTACLE FRAME OR EYEGLASS FRAMES 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