FDA 510(k)

TheraVision Ultrasound Ablation System and ACOUSTx Applicators

Номер K: K150019 · 2016-01-13

Дата решения2016-01-13

Код продуктаNTB

Консультативный комитетSU

РешениеSubstantially Equivalent

Описание устройства

TheraVision Ultrasound Ablation System and ACOUSTx Applicators is the device name listed in this FDA 510(k) record. The listed applicant is Acoustic Medsystems, Inc.. It received FDA 510(k) clearance on 2016-01-13 under 510(k) number K150019. The device is classified under product code NTB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the TheraVision Ultrasound Ablation System and ACOUSTx Applicators?

TheraVision Ultrasound Ablation System and ACOUSTx Applicators is a medical device that received FDA 510(k) clearance on 2016-01-13. The listed applicant is Acoustic Medsystems, Inc.. The 510(k) number is K150019.

When did TheraVision Ultrasound Ablation System and ACOUSTx Applicators receive FDA 510(k) clearance?

TheraVision Ultrasound Ablation System and ACOUSTx Applicators received FDA 510(k) clearance on 2016-01-13, under 510(k) number K150019.

Who is the listed applicant for TheraVision Ultrasound Ablation System and ACOUSTx Applicators?

The FDA 510(k) record lists Acoustic Medsystems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TheraVision Ultrasound Ablation System and ACOUSTx Applicators?

The FDA product code for TheraVision Ultrasound Ablation System and ACOUSTx Applicators is NTB.

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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