FDA 510(k)

JetCan® Pro Safety Huber Needle

Número K: K242763 · 2025-05-02

Data da decisão2025-05-02

Código do produtoFPA

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

JetCan® Pro Safety Huber Needle is the device name listed in this FDA 510(k) record. The listed applicant is Pfm Medical, Inc.. It received FDA 510(k) clearance on 2025-05-02 under 510(k) number K242763. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the JetCan® Pro Safety Huber Needle?

JetCan® Pro Safety Huber Needle is a medical device that received FDA 510(k) clearance on 2025-05-02. The listed applicant is Pfm Medical, Inc.. The 510(k) number is K242763.

When did JetCan® Pro Safety Huber Needle receive FDA 510(k) clearance?

JetCan® Pro Safety Huber Needle received FDA 510(k) clearance on 2025-05-02, under 510(k) number K242763.

Who is the listed applicant for JetCan® Pro Safety Huber Needle?

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

What is the FDA product code for JetCan® Pro Safety Huber Needle?

The FDA product code for JetCan® Pro Safety Huber Needle is FPA.

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Fonte oficial

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