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FDA 510(k)

OPTI-RAY SUNGLASSES

K-Number: K902414 · 1990-07-17

Decision Date1990-07-17
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTI-RAY SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Opti-Ray, Inc.. It received FDA 510(k) clearance on 1990-07-17 under 510(k) number K902414. 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 OPTI-RAY SUNGLASSES?

OPTI-RAY SUNGLASSES is a medical device that received FDA 510(k) clearance on 1990-07-17. The listed applicant is Opti-Ray, Inc.. The 510(k) number is K902414.

When did OPTI-RAY SUNGLASSES receive FDA 510(k) clearance?

OPTI-RAY SUNGLASSES received FDA 510(k) clearance on 1990-07-17, under 510(k) number K902414.

Who is the listed applicant for OPTI-RAY SUNGLASSES?

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

What is the FDA product code for OPTI-RAY SUNGLASSES?

The FDA product code for OPTI-RAY 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.

Other records listing Opti-Ray, Inc. as applicant

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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