FDA 510(k)

Multi-Link X2 ECG Cable and Lead Wire System

N.º K: K162432 · 2017-01-18

Fecha de decisión2017-01-18

Código de productoDSA

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Multi-Link X2 ECG Cable and Lead Wire System is the device name listed in this FDA 510(k) record. The listed applicant is Carefusion 2200, Inc.. It received FDA 510(k) clearance on 2017-01-18 under 510(k) number K162432. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Multi-Link X2 ECG Cable and Lead Wire System?

Multi-Link X2 ECG Cable and Lead Wire System is a medical device that received FDA 510(k) clearance on 2017-01-18. The listed applicant is Carefusion 2200, Inc.. The 510(k) number is K162432.

When did Multi-Link X2 ECG Cable and Lead Wire System receive FDA 510(k) clearance?

Multi-Link X2 ECG Cable and Lead Wire System received FDA 510(k) clearance on 2017-01-18, under 510(k) number K162432.

Who is the listed applicant for Multi-Link X2 ECG Cable and Lead Wire System?

The FDA 510(k) record lists Carefusion 2200, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multi-Link X2 ECG Cable and Lead Wire System?

The FDA product code for Multi-Link X2 ECG Cable and Lead Wire System is DSA.

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

Otros registros que enlistan a Carefusion 2200, Inc. como solicitante

K210324V. Mueller Cosgrove Flex Clamps, Model Number-CV1033, CV1061, CV1133, CV1161, CV1186 K163615Snowden-Pencer MicroLap 3mm Laparoscopic Instruments K160764AirLife Autofill Humidification Chamber K153554Genesis Low Temperature Reusable Rigid Container System K151036Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments

Dispositivos relacionados (Código: DSA)

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.