FDA 510(k)

BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx

N.º K: K230238 · 2023-03-31

SolicitanteShenzhen Bioeasy Biotechnology Co., Ltd.

Fecha de decisión2023-03-31

Código de productoDJG

Comité asesorTX

DecisiónSubstantially Equivalent

Resumen del dispositivo

BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Bioeasy Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2023-03-31 under 510(k) number K230238. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx?

BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx is a medical device that received FDA 510(k) clearance on 2023-03-31. The listed applicant is Shenzhen Bioeasy Biotechnology Co., Ltd.. The 510(k) number is K230238.

When did BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx receive FDA 510(k) clearance?

BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx received FDA 510(k) clearance on 2023-03-31, under 510(k) number K230238.

Who is the listed applicant for BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx?

The FDA 510(k) record lists Shenzhen Bioeasy Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx?

The FDA product code for BIOEASY™ U-Catch MAX Multi-Drug Test Cup, BIOEASY™ U-Catch MAX Multi-Drug Test Cup Rx is DJG.

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Otros registros que enlistan a Shenzhen Bioeasy Biotechnology Co., Ltd. como solicitante

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Fuente oficial

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