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FDA 510(k)

NON-PRESCRIPTION SUGLASSES

K-Number: K932814 · 1993-09-20

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

Device Summary

NON-PRESCRIPTION SUGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Sun Style Intl. Corp.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K932814. 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 NON-PRESCRIPTION SUGLASSES?

NON-PRESCRIPTION SUGLASSES is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Sun Style Intl. Corp.. The 510(k) number is K932814.

When did NON-PRESCRIPTION SUGLASSES receive FDA 510(k) clearance?

NON-PRESCRIPTION SUGLASSES received FDA 510(k) clearance on 1993-09-20, under 510(k) number K932814.

Who is the listed applicant for NON-PRESCRIPTION SUGLASSES?

The FDA 510(k) record lists Sun Style Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NON-PRESCRIPTION SUGLASSES?

The FDA product code for NON-PRESCRIPTION SUGLASSES 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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