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FDA 510(k)

SINCLAIR NON-PRESCRIPTION SUNGLASSES

K-Number: K954393 · 1995-10-25

Decision Date1995-10-25
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SINCLAIR NON-PRESCRIPTION SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Sinclair Corp.. It received FDA 510(k) clearance on 1995-10-25 under 510(k) number K954393. 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 SINCLAIR NON-PRESCRIPTION SUNGLASSES?

SINCLAIR NON-PRESCRIPTION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1995-10-25. The listed applicant is Sinclair Corp.. The 510(k) number is K954393.

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

SINCLAIR NON-PRESCRIPTION SUNGLASSES received FDA 510(k) clearance on 1995-10-25, under 510(k) number K954393.

Who is the listed applicant for SINCLAIR NON-PRESCRIPTION SUNGLASSES?

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

What is the FDA product code for SINCLAIR NON-PRESCRIPTION SUNGLASSES?

The FDA product code for SINCLAIR NON-PRESCRIPTION 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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