FDA 510(k)

Model WP-3840 and WP-3040

N.º K: K173848 · 2018-08-07

Fecha de decisión2018-08-07

Código de productoIYE

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Model WP-3840 and WP-3040 is the device name listed in this FDA 510(k) record. The listed applicant is Cnmc Co., Inc.. It received FDA 510(k) clearance on 2018-08-07 under 510(k) number K173848. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Model WP-3840 and WP-3040?

Model WP-3840 and WP-3040 is a medical device that received FDA 510(k) clearance on 2018-08-07. The listed applicant is Cnmc Co., Inc.. The 510(k) number is K173848.

When did Model WP-3840 and WP-3040 receive FDA 510(k) clearance?

Model WP-3840 and WP-3040 received FDA 510(k) clearance on 2018-08-07, under 510(k) number K173848.

Who is the listed applicant for Model WP-3840 and WP-3040?

The FDA 510(k) record lists Cnmc Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Model WP-3840 and WP-3040?

The FDA product code for Model WP-3840 and WP-3040 is IYE.

Ensayos clínicos relacionados

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Dispositivos relacionados (Código: IYE)

K261865AerFrame™ Alignment Laser Box (LBV2)Stabilix, LLC K261718EZFluence (RADEZ V2)Radformation, Inc.K260733MRIA Radiation Therapy Information System (MRIA)Manteia Technologies Co., Ltd.K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SA K253004LUNA 3DLap GmbH Laser Applikationen

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.