FDA 510(k)

Introcan Safety® 2 IV Catheter

Número K: K241845 · 2024-07-26

Data da decisão2024-07-26

Código do produtoFOZ

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Introcan Safety® 2 IV Catheter is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2024-07-26 under 510(k) number K241845. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Introcan Safety® 2 IV Catheter?

Introcan Safety® 2 IV Catheter is a medical device that received FDA 510(k) clearance on 2024-07-26. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K241845.

When did Introcan Safety® 2 IV Catheter receive FDA 510(k) clearance?

Introcan Safety® 2 IV Catheter received FDA 510(k) clearance on 2024-07-26, under 510(k) number K241845.

Who is the listed applicant for Introcan Safety® 2 IV Catheter?

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

What is the FDA product code for Introcan Safety® 2 IV Catheter?

The FDA product code for Introcan Safety® 2 IV Catheter is FOZ.

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Fonte oficial

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