SUNGLASSES AND SPECTACLE FRAMES
K-Number: K944644 · 1994-11-15
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Device Summary
Frequently Asked Questions
What is the SUNGLASSES AND SPECTACLE FRAMES?
SUNGLASSES AND SPECTACLE FRAMES is a medical device that received FDA 510(k) clearance on 1994-11-15. The listed applicant is Hung Wai Metal Manufactory. The 510(k) number is K944644.
When did SUNGLASSES AND SPECTACLE FRAMES receive FDA 510(k) clearance?
SUNGLASSES AND SPECTACLE FRAMES received FDA 510(k) clearance on 1994-11-15, under 510(k) number K944644.
Who is the listed applicant for SUNGLASSES AND SPECTACLE FRAMES?
The FDA 510(k) record lists Hung Wai Metal Manufactory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUNGLASSES AND SPECTACLE FRAMES?
The FDA product code for SUNGLASSES AND SPECTACLE FRAMES is HQY.
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: HQY)
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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