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FDA 510(k)

UV Lamps for Sunlamp Products

Número K: K180581 · 2018-06-22

RequerenteFeilo Sylvania Germany GmbH
Data da decisão2018-06-22
Código do produtoLEJ
Comité consultivoSU
DecisãoSubstantially Equivalent

Resumo do dispositivo

UV Lamps for Sunlamp Products is the device name listed in this FDA 510(k) record. The listed applicant is Feilo Sylvania Germany GmbH. It received FDA 510(k) clearance on 2018-06-22 under 510(k) number K180581. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the UV Lamps for Sunlamp Products?

UV Lamps for Sunlamp Products is a medical device that received FDA 510(k) clearance on 2018-06-22. The listed applicant is Feilo Sylvania Germany GmbH. The 510(k) number is K180581.

When did UV Lamps for Sunlamp Products receive FDA 510(k) clearance?

UV Lamps for Sunlamp Products received FDA 510(k) clearance on 2018-06-22, under 510(k) number K180581.

Who is the listed applicant for UV Lamps for Sunlamp Products?

The FDA 510(k) record lists Feilo Sylvania Germany GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UV Lamps for Sunlamp Products?

The FDA product code for UV Lamps for Sunlamp Products is LEJ.

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