FLOATS SUNGLASSES
K-Number: K932151 · 1994-01-03
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Device Summary
Frequently Asked Questions
What is the FLOATS SUNGLASSES?
FLOATS SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-01-03. The listed applicant is Floats, Inc.. The 510(k) number is K932151.
When did FLOATS SUNGLASSES receive FDA 510(k) clearance?
FLOATS SUNGLASSES received FDA 510(k) clearance on 1994-01-03, under 510(k) number K932151.
Who is the listed applicant for FLOATS SUNGLASSES?
The FDA 510(k) record lists Floats, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLOATS SUNGLASSES?
The FDA product code for FLOATS 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.
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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