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FDA 510(k)

MULTIPLE -SPECTACLE FRAMES/SUNGLASSES

K-Number: K935798 · 1994-02-16

Decision Date1994-02-16
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULTIPLE -SPECTACLE FRAMES/SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Tae Kyung Optical Co., Inc.. It received FDA 510(k) clearance on 1994-02-16 under 510(k) number K935798. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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