FDA 510(k)

BAHADIR STERILIZATION CONTAINERS

Номер K: K233578 · 2024-03-22

Дата решения2024-03-22

Код продуктаKCT

Консультативный комитетHO

РешениеSubstantially Equivalent

Описание устройства

BAHADIR STERILIZATION CONTAINERS is the device name listed in this FDA 510(k) record. The listed applicant is Bahadir USA, LLC. It received FDA 510(k) clearance on 2024-03-22 under 510(k) number K233578. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the BAHADIR STERILIZATION CONTAINERS?

BAHADIR STERILIZATION CONTAINERS is a medical device that received FDA 510(k) clearance on 2024-03-22. The listed applicant is Bahadir USA, LLC. The 510(k) number is K233578.

When did BAHADIR STERILIZATION CONTAINERS receive FDA 510(k) clearance?

BAHADIR STERILIZATION CONTAINERS received FDA 510(k) clearance on 2024-03-22, under 510(k) number K233578.

Who is the listed applicant for BAHADIR STERILIZATION CONTAINERS?

The FDA 510(k) record lists Bahadir USA, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAHADIR STERILIZATION CONTAINERS?

The FDA product code for BAHADIR STERILIZATION CONTAINERS is KCT.

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: KCT)

K253988LiteSet TraysNobel Biocare AB K261935Surgical and Prosthetic TraysDentsply Sirona, Inc.K253187SteriBest® Sterilization Tray SystemMastel Surgical K252854SteriTite Container System with MediTray ProductsCase Medical, Inc.K260726Straumann® ProClean™ Cassette (041.800 ; 041.801)Institut Straumann AG K253791PUREVUE™ Quick Connect Cannula System Tray; PUREVUE™ Quick Connect Cannula System LidDePuy Mitek, Inc.

Официальный источник

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