FDA 510(k)

AIK Sterile Acupuncture Needles for Single Use

Номер K: K162566 · 2017-05-11

ЗаявительChangchun Aik Medical Devices Co., Ltd.

Дата решения2017-05-11

Код продуктаMQX

Консультативный комитетHO

РешениеSubstantially Equivalent

Описание устройства

AIK Sterile Acupuncture Needles for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Changchun Aik Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2017-05-11 under 510(k) number K162566. The device is classified under product code MQX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the AIK Sterile Acupuncture Needles for Single Use?

AIK Sterile Acupuncture Needles for Single Use is a medical device that received FDA 510(k) clearance on 2017-05-11. The listed applicant is Changchun Aik Medical Devices Co., Ltd.. The 510(k) number is K162566.

When did AIK Sterile Acupuncture Needles for Single Use receive FDA 510(k) clearance?

AIK Sterile Acupuncture Needles for Single Use received FDA 510(k) clearance on 2017-05-11, under 510(k) number K162566.

Who is the listed applicant for AIK Sterile Acupuncture Needles for Single Use?

The FDA 510(k) record lists Changchun Aik Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIK Sterile Acupuncture Needles for Single Use?

The FDA product code for AIK Sterile Acupuncture Needles for Single Use is MQX.

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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