FDA 510(k)

Introcan Safety® Deep Access XL IV Catheter

Número K: K253235 · 2026-05-15

Data da decisão2026-05-15

Código do produtoFOZ

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Introcan Safety® Deep Access XL 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 2026-05-15 under 510(k) number K253235. 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® Deep Access XL IV Catheter?

Introcan Safety® Deep Access XL IV Catheter is a medical device that received FDA 510(k) clearance on 2026-05-15. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K253235.

When did Introcan Safety® Deep Access XL IV Catheter receive FDA 510(k) clearance?

Introcan Safety® Deep Access XL IV Catheter received FDA 510(k) clearance on 2026-05-15, under 510(k) number K253235.

Who is the listed applicant for Introcan Safety® Deep Access XL 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® Deep Access XL IV Catheter?

The FDA product code for Introcan Safety® Deep Access XL IV Catheter is FOZ.

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