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FDA 510(k)

SUNGLASSES OR MULTIPLE

K-Number: K960890 · 1996-04-10

Decision Date1996-04-10
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNGLASSES OR MULTIPLE is the device name listed in this FDA 510(k) record. The listed applicant is Outdoor Action Wear Specialties. It received FDA 510(k) clearance on 1996-04-10 under 510(k) number K960890. 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 SUNGLASSES OR MULTIPLE?

SUNGLASSES OR MULTIPLE is a medical device that received FDA 510(k) clearance on 1996-04-10. The listed applicant is Outdoor Action Wear Specialties. The 510(k) number is K960890.

When did SUNGLASSES OR MULTIPLE receive FDA 510(k) clearance?

SUNGLASSES OR MULTIPLE received FDA 510(k) clearance on 1996-04-10, under 510(k) number K960890.

Who is the listed applicant for SUNGLASSES OR MULTIPLE?

The FDA 510(k) record lists Outdoor Action Wear Specialties as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNGLASSES OR MULTIPLE?

The FDA product code for SUNGLASSES OR MULTIPLE 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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