DESERT SHIELD SUNGLASSES
K-Number: K912863 · 1991-09-25
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Device Summary
Frequently Asked Questions
What is the DESERT SHIELD SUNGLASSES?
DESERT SHIELD SUNGLASSES is a medical device that received FDA 510(k) clearance on 1991-09-25. The listed applicant is Command Marketing Corp.. The 510(k) number is K912863.
When did DESERT SHIELD SUNGLASSES receive FDA 510(k) clearance?
DESERT SHIELD SUNGLASSES received FDA 510(k) clearance on 1991-09-25, under 510(k) number K912863.
Who is the listed applicant for DESERT SHIELD SUNGLASSES?
The FDA 510(k) record lists Command Marketing Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DESERT SHIELD SUNGLASSES?
The FDA product code for DESERT SHIELD 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 Command Marketing 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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