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FDA 510(k)

OAKLEY, INC SUNGLASSES

K-Number: K961268 · 1996-04-24

ApplicantOakley, Inc.
Decision Date1996-04-24
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OAKLEY, INC SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Oakley, Inc.. It received FDA 510(k) clearance on 1996-04-24 under 510(k) number K961268. 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 OAKLEY, INC SUNGLASSES?

OAKLEY, INC SUNGLASSES is a medical device that received FDA 510(k) clearance on 1996-04-24. The listed applicant is Oakley, Inc.. The 510(k) number is K961268.

When did OAKLEY, INC SUNGLASSES receive FDA 510(k) clearance?

OAKLEY, INC SUNGLASSES received FDA 510(k) clearance on 1996-04-24, under 510(k) number K961268.

Who is the listed applicant for OAKLEY, INC SUNGLASSES?

The FDA 510(k) record lists Oakley, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OAKLEY, INC SUNGLASSES?

The FDA product code for OAKLEY, INC SUNGLASSES is HQY.

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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.

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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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