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FDA 510(k)

ACRYLIC READING AND POLYCARBONATE LENSES SUNGLASSES

K-Number: K962279 · 1996-08-26

Decision Date1996-08-26
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ACRYLIC READING AND POLYCARBONATE LENSES SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Jane Fui Optical Co., Ltd.. It received FDA 510(k) clearance on 1996-08-26 under 510(k) number K962279. 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 ACRYLIC READING AND POLYCARBONATE LENSES SUNGLASSES?

ACRYLIC READING AND POLYCARBONATE LENSES SUNGLASSES is a medical device that received FDA 510(k) clearance on 1996-08-26. The listed applicant is Jane Fui Optical Co., Ltd.. The 510(k) number is K962279.

When did ACRYLIC READING AND POLYCARBONATE LENSES SUNGLASSES receive FDA 510(k) clearance?

ACRYLIC READING AND POLYCARBONATE LENSES SUNGLASSES received FDA 510(k) clearance on 1996-08-26, under 510(k) number K962279.

Who is the listed applicant for ACRYLIC READING AND POLYCARBONATE LENSES SUNGLASSES?

The FDA 510(k) record lists Jane Fui Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACRYLIC READING AND POLYCARBONATE LENSES SUNGLASSES?

The FDA product code for ACRYLIC READING AND POLYCARBONATE LENSES 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.

Other records listing Jane Fui Optical Co., Ltd. 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: 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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