FINE OPTICS SUNGLASSES
K-Number: K933938 · 1994-01-06
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Device Summary
Frequently Asked Questions
What is the FINE OPTICS SUNGLASSES?
FINE OPTICS SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-01-06. The listed applicant is Fine Optics, Inc.. The 510(k) number is K933938.
When did FINE OPTICS SUNGLASSES receive FDA 510(k) clearance?
FINE OPTICS SUNGLASSES received FDA 510(k) clearance on 1994-01-06, under 510(k) number K933938.
Who is the listed applicant for FINE OPTICS SUNGLASSES?
The FDA 510(k) record lists Fine Optics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FINE OPTICS SUNGLASSES?
The FDA product code for FINE OPTICS 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 Fine Optics, Inc. 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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