FDA 510(k)

Radial Jaw 4 Pulmonary Biopsy Forceps

Número K: K252921 · 2025-09-26

Data da decisão2025-09-26

Código do produtoBWH

Comité consultivoEN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Radial Jaw 4 Pulmonary Biopsy Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2025-09-26 under 510(k) number K252921. The device is classified under product code BWH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Radial Jaw 4 Pulmonary Biopsy Forceps?

Radial Jaw 4 Pulmonary Biopsy Forceps is a medical device that received FDA 510(k) clearance on 2025-09-26. The listed applicant is Boston Scientific Corporation. The 510(k) number is K252921.

When did Radial Jaw 4 Pulmonary Biopsy Forceps receive FDA 510(k) clearance?

Radial Jaw 4 Pulmonary Biopsy Forceps received FDA 510(k) clearance on 2025-09-26, under 510(k) number K252921.

Who is the listed applicant for Radial Jaw 4 Pulmonary Biopsy Forceps?

The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Radial Jaw 4 Pulmonary Biopsy Forceps?

The FDA product code for Radial Jaw 4 Pulmonary Biopsy Forceps is BWH.

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