GIRARD SUNGLASSES (NON-PRESCRIPTION)
K-Number: K861759 · 1986-06-09
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Device Summary
Frequently Asked Questions
What is the GIRARD SUNGLASSES (NON-PRESCRIPTION)?
GIRARD SUNGLASSES (NON-PRESCRIPTION) is a medical device that received FDA 510(k) clearance on 1986-06-09. The listed applicant is H. Girard S.A.. The 510(k) number is K861759.
When did GIRARD SUNGLASSES (NON-PRESCRIPTION) receive FDA 510(k) clearance?
GIRARD SUNGLASSES (NON-PRESCRIPTION) received FDA 510(k) clearance on 1986-06-09, under 510(k) number K861759.
Who is the listed applicant for GIRARD SUNGLASSES (NON-PRESCRIPTION)?
The FDA 510(k) record lists H. Girard S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GIRARD SUNGLASSES (NON-PRESCRIPTION)?
The FDA product code for GIRARD SUNGLASSES (NON-PRESCRIPTION) is HQG.
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: HQG)
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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