H. Girard S.A.
FranceFDA 510(k) applicant, unverified
- Devices
- 1
What H. Girard S.A. makes
H. Girard S.A. manufactures non-prescription sunglasses designed for general eye protection and UV radiation blocking.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Girard Sunglasses (Non-Prescription) Ref K861759
510(k) 510(k)
Frequently asked questions
How many devices does H. Girard S.A. have in the registry?
The registry currently lists 1 device for H. Girard S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list H. Girard S.A.'s devices?
Among its 1 most recently registered device, H. Girard S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do H. Girard S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for H. Girard S.A.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from H. Girard S.A. in the registry?
The most recently registered devices listed for H. Girard S.A. include GIRARD SUNGLASSES (NON-PRESCRIPTION).