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FDA 510(k)

MISTRAL SUNGLASSES

K-Number: K960668 · 1996-05-31

Decision Date1996-05-31
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MISTRAL SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Mistral Optical. It received FDA 510(k) clearance on 1996-05-31 under 510(k) number K960668. 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 MISTRAL SUNGLASSES?

MISTRAL SUNGLASSES is a medical device that received FDA 510(k) clearance on 1996-05-31. The listed applicant is Mistral Optical. The 510(k) number is K960668.

When did MISTRAL SUNGLASSES receive FDA 510(k) clearance?

MISTRAL SUNGLASSES received FDA 510(k) clearance on 1996-05-31, under 510(k) number K960668.

Who is the listed applicant for MISTRAL SUNGLASSES?

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

What is the FDA product code for MISTRAL SUNGLASSES?

The FDA product code for MISTRAL 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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