FDA 510(k)

NailLift

Número K: K230841 · 2024-01-22

Data da decisão2024-01-22

Código do produtoMQZ

DecisãoSubstantially Equivalent

Resumo do dispositivo

NailLift is the device name listed in this FDA 510(k) record. The listed applicant is Jps Corporation. It received FDA 510(k) clearance on 2024-01-22 under 510(k) number K230841. The device is classified under product code MQZ. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the NailLift?

NailLift is a medical device that received FDA 510(k) clearance on 2024-01-22. The listed applicant is Jps Corporation. The 510(k) number is K230841.

When did NailLift receive FDA 510(k) clearance?

NailLift received FDA 510(k) clearance on 2024-01-22, under 510(k) number K230841.

Who is the listed applicant for NailLift?

The FDA 510(k) record lists Jps Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NailLift?

The FDA product code for NailLift is MQZ.

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Fonte oficial

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