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FDA 510(k)

SUNGLASSES

K-Number: K925428 · 1993-09-20

Decision Date1993-09-20
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Dallas Handbag Co.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K925428. 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?

SUNGLASSES is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Dallas Handbag Co.. The 510(k) number is K925428.

When did SUNGLASSES receive FDA 510(k) clearance?

SUNGLASSES received FDA 510(k) clearance on 1993-09-20, under 510(k) number K925428.

Who is the listed applicant for SUNGLASSES?

The FDA 510(k) record lists Dallas Handbag Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNGLASSES?

The FDA product code for 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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