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FDA 510(k)

SUNGLASSES (NON PRESCRIPTION)

K-Number: K941280 · 1994-05-17

Decision Date1994-05-17
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNGLASSES (NON PRESCRIPTION) is the device name listed in this FDA 510(k) record. The listed applicant is Autotime Industry, Inc.. It received FDA 510(k) clearance on 1994-05-17 under 510(k) number K941280. 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 (NON PRESCRIPTION)?

SUNGLASSES (NON PRESCRIPTION) is a medical device that received FDA 510(k) clearance on 1994-05-17. The listed applicant is Autotime Industry, Inc.. The 510(k) number is K941280.

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

SUNGLASSES (NON PRESCRIPTION) received FDA 510(k) clearance on 1994-05-17, under 510(k) number K941280.

Who is the listed applicant for SUNGLASSES (NON PRESCRIPTION)?

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

What is the FDA product code for SUNGLASSES (NON PRESCRIPTION)?

The FDA product code for SUNGLASSES (NON PRESCRIPTION) 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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