FDA 510(k)

Michler-Kapp Cardiovascular Vent Catheter

Номер K: K200289 · 2021-01-28

Дата решения2021-01-28

Код продуктаDWF

Консультативный комитетCV

РешениеSubstantially Equivalent

Описание устройства

Michler-Kapp Cardiovascular Vent Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Kapp Surgical Instrument, Inc.. It received FDA 510(k) clearance on 2021-01-28 under 510(k) number K200289. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the Michler-Kapp Cardiovascular Vent Catheter?

Michler-Kapp Cardiovascular Vent Catheter is a medical device that received FDA 510(k) clearance on 2021-01-28. The listed applicant is Kapp Surgical Instrument, Inc.. The 510(k) number is K200289.

When did Michler-Kapp Cardiovascular Vent Catheter receive FDA 510(k) clearance?

Michler-Kapp Cardiovascular Vent Catheter received FDA 510(k) clearance on 2021-01-28, under 510(k) number K200289.

Who is the listed applicant for Michler-Kapp Cardiovascular Vent Catheter?

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

What is the FDA product code for Michler-Kapp Cardiovascular Vent Catheter?

The FDA product code for Michler-Kapp Cardiovascular Vent Catheter is DWF.

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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Связанные устройства (Код: DWF)

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Официальный источник

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