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FDA 510(k)

GIRARD SUNGLASSES (NON-PRESCRIPTION)

K-Number: K861759 · 1986-06-09

Decision Date1986-06-09
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GIRARD SUNGLASSES (NON-PRESCRIPTION) is the device name listed in this FDA 510(k) record. The listed applicant is H. Girard S.A.. It received FDA 510(k) clearance on 1986-06-09 under 510(k) number K861759. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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