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FDA 510(k)

ZONG RONG SUNGLASSES

K-Number: K955287 · 1996-01-29

Decision Date1996-01-29
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ZONG RONG SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Yuu Yeng Enterprise Co., Ltd.. It received FDA 510(k) clearance on 1996-01-29 under 510(k) number K955287. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZONG RONG SUNGLASSES?

ZONG RONG SUNGLASSES is a medical device that received FDA 510(k) clearance on 1996-01-29. The listed applicant is Yuu Yeng Enterprise Co., Ltd.. The 510(k) number is K955287.

When did ZONG RONG SUNGLASSES receive FDA 510(k) clearance?

ZONG RONG SUNGLASSES received FDA 510(k) clearance on 1996-01-29, under 510(k) number K955287.

Who is the listed applicant for ZONG RONG SUNGLASSES?

The FDA 510(k) record lists Yuu Yeng Enterprise Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZONG RONG SUNGLASSES?

The FDA product code for ZONG RONG SUNGLASSES 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

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