BULLET SUNGLASSES
K-Number: K900383 · 1990-02-13
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Device Summary
Frequently Asked Questions
What is the BULLET SUNGLASSES?
BULLET 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 K900383.
When did BULLET SUNGLASSES receive FDA 510(k) clearance?
BULLET SUNGLASSES received FDA 510(k) clearance on 1990-02-13, under 510(k) number K900383.
Who is the listed applicant for BULLET 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 BULLET SUNGLASSES?
The FDA product code for BULLET 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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