SPECTACLE SUN GLASSES (NON PRESCRIPTION)
K-Number: K934081 · 1993-10-18
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Device Summary
Frequently Asked Questions
What is the SPECTACLE SUN GLASSES (NON PRESCRIPTION)?
SPECTACLE SUN GLASSES (NON PRESCRIPTION) is a medical device that received FDA 510(k) clearance on 1993-10-18. The listed applicant is South American Optical, Inc.. The 510(k) number is K934081.
When did SPECTACLE SUN GLASSES (NON PRESCRIPTION) receive FDA 510(k) clearance?
SPECTACLE SUN GLASSES (NON PRESCRIPTION) received FDA 510(k) clearance on 1993-10-18, under 510(k) number K934081.
Who is the listed applicant for SPECTACLE SUN GLASSES (NON PRESCRIPTION)?
The FDA 510(k) record lists South American Optical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPECTACLE SUN GLASSES (NON PRESCRIPTION)?
The FDA product code for SPECTACLE SUN GLASSES (NON PRESCRIPTION) 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 South American Optical, 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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