BLUBLOCKER SUNGLASSES
K-Number: K900382 · 1990-02-13
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Device Summary
Frequently Asked Questions
What is the BLUBLOCKER SUNGLASSES?
BLUBLOCKER 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 K900382.
When did BLUBLOCKER SUNGLASSES receive FDA 510(k) clearance?
BLUBLOCKER SUNGLASSES received FDA 510(k) clearance on 1990-02-13, under 510(k) number K900382.
Who is the listed applicant for BLUBLOCKER 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 BLUBLOCKER SUNGLASSES?
The FDA product code for BLUBLOCKER 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.
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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