FDA 510(k)

Vital Sleep

Número K: K201719 · 2021-01-14

RequerenteThe Snore Reliever Company, LLC

Data da decisão2021-01-14

Código do produtoLRK

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vital Sleep is the device name listed in this FDA 510(k) record. The listed applicant is The Snore Reliever Company, LLC. It received FDA 510(k) clearance on 2021-01-14 under 510(k) number K201719. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Vital Sleep?

Vital Sleep is a medical device that received FDA 510(k) clearance on 2021-01-14. The listed applicant is The Snore Reliever Company, LLC. The 510(k) number is K201719.

When did Vital Sleep receive FDA 510(k) clearance?

Vital Sleep received FDA 510(k) clearance on 2021-01-14, under 510(k) number K201719.

Who is the listed applicant for Vital Sleep?

The FDA 510(k) record lists The Snore Reliever Company, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vital Sleep?

The FDA product code for Vital Sleep is LRK.

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Fonte oficial

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