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FDA 510(k)

COLORVISION SUNGLASSES

K-Number: K900381 · 1990-02-13

Decision Date1990-02-13
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

COLORVISION SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Blublocker Corp.. It received FDA 510(k) clearance on 1990-02-13 under 510(k) number K900381. 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 COLORVISION SUNGLASSES?

COLORVISION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1990-02-13. The listed applicant is Blublocker Corp.. The 510(k) number is K900381.

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

COLORVISION SUNGLASSES received FDA 510(k) clearance on 1990-02-13, under 510(k) number K900381.

Who is the listed applicant for COLORVISION SUNGLASSES?

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

What is the FDA product code for COLORVISION SUNGLASSES?

The FDA product code for COLORVISION 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 Blublocker Corp. 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.

View all 7 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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