SUNGLASSES (NON-PRESCRIPTION)
K-Number: K934374 · 1993-12-08
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Device Summary
Frequently Asked Questions
What is the SUNGLASSES (NON-PRESCRIPTION)?
SUNGLASSES (NON-PRESCRIPTION) is a medical device that received FDA 510(k) clearance on 1993-12-08. The listed applicant is Immmex Company , Ltd.. The 510(k) number is K934374.
When did SUNGLASSES (NON-PRESCRIPTION) receive FDA 510(k) clearance?
SUNGLASSES (NON-PRESCRIPTION) received FDA 510(k) clearance on 1993-12-08, under 510(k) number K934374.
Who is the listed applicant for SUNGLASSES (NON-PRESCRIPTION)?
The FDA 510(k) record lists Immmex Company , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUNGLASSES (NON-PRESCRIPTION)?
The FDA product code for SUNGLASSES (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.
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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