Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

FDA 510(k)

SKIN CARE

N.º K: K152736 · 2016-02-25

SolicitanteC.I.S, Ltd.
Fecha de decisión2016-02-25
Código de productoGEX
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

SKIN CARE is the device name listed in this FDA 510(k) record. The listed applicant is C.I.S, Ltd.. It received FDA 510(k) clearance on 2016-02-25 under 510(k) number K152736. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the SKIN CARE?

SKIN CARE is a medical device that received FDA 510(k) clearance on 2016-02-25. The listed applicant is C.I.S, Ltd.. The 510(k) number is K152736.

When did SKIN CARE receive FDA 510(k) clearance?

SKIN CARE received FDA 510(k) clearance on 2016-02-25, under 510(k) number K152736.

Who is the listed applicant for SKIN CARE?

The FDA 510(k) record lists C.I.S, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKIN CARE?

The FDA product code for SKIN CARE is GEX. This falls under the Gastroenterology category.

Dispositivos relacionados (Código: GEX)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K254199PicoreMax (PicoreMax)BLUECORE COMPANY Co., Ltd.K252723Dynamis Pro FamilyFotona D.O.O.K241973SmartIPL_NI SystemLumenis Be, Ltd.K261047Dental Diode Laser Device (Laser-Pen)Guilin Kevin Peter Technology Co., Ltd.K261817Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.K261673LED Therapy Device (QLXY-01)Beijing Nubway S&T Co., Ltd.

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.

↑