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FDA 510(k)

SUNGLASSES, NONPRESCRIPTION

K-Number: K951131 · 1995-05-10

ApplicantGold, Inc.
Decision Date1995-05-10
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNGLASSES, NONPRESCRIPTION is the device name listed in this FDA 510(k) record. The listed applicant is Gold, Inc.. It received FDA 510(k) clearance on 1995-05-10 under 510(k) number K951131. 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, NONPRESCRIPTION?

SUNGLASSES, NONPRESCRIPTION is a medical device that received FDA 510(k) clearance on 1995-05-10. The listed applicant is Gold, Inc.. The 510(k) number is K951131.

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

SUNGLASSES, NONPRESCRIPTION received FDA 510(k) clearance on 1995-05-10, under 510(k) number K951131.

Who is the listed applicant for SUNGLASSES, NONPRESCRIPTION?

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

What is the FDA product code for SUNGLASSES, NONPRESCRIPTION?

The FDA product code for SUNGLASSES, NONPRESCRIPTION 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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