MULTIPLE -SPECTACLE FRAMES/SUNGLASSES
K-Number: K935798 · 1994-02-16
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Device Summary
Frequently Asked Questions
What is the MULTIPLE -SPECTACLE FRAMES/SUNGLASSES?
MULTIPLE -SPECTACLE FRAMES/SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-02-16. The listed applicant is Tae Kyung Optical Co., Inc.. The 510(k) number is K935798.
When did MULTIPLE -SPECTACLE FRAMES/SUNGLASSES receive FDA 510(k) clearance?
MULTIPLE -SPECTACLE FRAMES/SUNGLASSES received FDA 510(k) clearance on 1994-02-16, under 510(k) number K935798.
Who is the listed applicant for MULTIPLE -SPECTACLE FRAMES/SUNGLASSES?
The FDA 510(k) record lists Tae Kyung Optical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTIPLE -SPECTACLE FRAMES/SUNGLASSES?
The FDA product code for MULTIPLE -SPECTACLE FRAMES/SUNGLASSES 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.
Other records listing Tae Kyung Optical Co., Inc. as applicant
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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