FDA 510(k)

NeedleSmart Professional (NS Pro)

Номер K: K202073 · 2021-03-25

Дата решения2021-03-25

Код продуктаMTV

Консультативный комитетHO

РешениеSubstantially Equivalent

Описание устройства

NeedleSmart Professional (NS Pro) is the device name listed in this FDA 510(k) record. The listed applicant is Needlesmart Limited. It received FDA 510(k) clearance on 2021-03-25 under 510(k) number K202073. The device is classified under product code MTV. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the NeedleSmart Professional (NS Pro)?

NeedleSmart Professional (NS Pro) is a medical device that received FDA 510(k) clearance on 2021-03-25. The listed applicant is Needlesmart Limited. The 510(k) number is K202073.

When did NeedleSmart Professional (NS Pro) receive FDA 510(k) clearance?

NeedleSmart Professional (NS Pro) received FDA 510(k) clearance on 2021-03-25, under 510(k) number K202073.

Who is the listed applicant for NeedleSmart Professional (NS Pro)?

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

What is the FDA product code for NeedleSmart Professional (NS Pro)?

The FDA product code for NeedleSmart Professional (NS Pro) is MTV.

Связанные клинические исследования

Связанные записи сопоставляются автоматически на основании названий, кодов продукции или иных метаданных. Сопоставление не подтверждает клиническую, научную, корпоративную или регуляторную связь; ознакомьтесь с официальными источниками по ссылкам.

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