FDA 510(k)

Huahong Sharps Container (HHR-I, HHR-II)

N.º K: K260845 · 2026-08-05

SolicitanteTianjin Huahong Technology Co., Ltd.

Fecha de decisión2026-08-05

Código de productoMMK

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Huahong Sharps Container (HHR-I, HHR-II) is the device name listed in this FDA 510(k) record. The listed applicant is Tianjin Huahong Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-08-05 under 510(k) number K260845. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Huahong Sharps Container (HHR-I, HHR-II)?

Huahong Sharps Container (HHR-I, HHR-II) is a medical device that received FDA 510(k) clearance on 2026-08-05. The listed applicant is Tianjin Huahong Technology Co., Ltd.. The 510(k) number is K260845.

When did Huahong Sharps Container (HHR-I, HHR-II) receive FDA 510(k) clearance?

Huahong Sharps Container (HHR-I, HHR-II) received FDA 510(k) clearance on 2026-08-05, under 510(k) number K260845.

Who is the listed applicant for Huahong Sharps Container (HHR-I, HHR-II)?

The FDA 510(k) record lists Tianjin Huahong Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Huahong Sharps Container (HHR-I, HHR-II)?

The FDA product code for Huahong Sharps Container (HHR-I, HHR-II) is MMK.

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Otros registros que enlistan a Tianjin Huahong Technology Co., Ltd. como solicitante

K262526Safety lancet (XL)K262135Lancing device K262211Lancet K260191Safety lancet (XXXVII)K252490Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)K253706Lancing device (HH-XV-T)

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Dispositivos relacionados (Código: MMK)

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.