FDA 510(k)

Disposable Bipolar Forceps

N.º K: K232703 · 2024-03-06

SolicitanteJiangsu Hope Biomedical Science & Technology Co., Ltd.

Fecha de decisión2024-03-06

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Disposable Bipolar Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Hope Biomedical Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-03-06 under 510(k) number K232703. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Disposable Bipolar Forceps?

Disposable Bipolar Forceps is a medical device that received FDA 510(k) clearance on 2024-03-06. The listed applicant is Jiangsu Hope Biomedical Science & Technology Co., Ltd.. The 510(k) number is K232703.

When did Disposable Bipolar Forceps receive FDA 510(k) clearance?

Disposable Bipolar Forceps received FDA 510(k) clearance on 2024-03-06, under 510(k) number K232703.

Who is the listed applicant for Disposable Bipolar Forceps?

The FDA 510(k) record lists Jiangsu Hope Biomedical Science & Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Bipolar Forceps?

The FDA product code for Disposable Bipolar Forceps is GEI.

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Otros registros que enlistan a Jiangsu Hope Biomedical Science & Technology Co., Ltd. como solicitante

K231615Disposable Endoscopic Bipolar

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Fuente oficial

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