FDA 510(k)

Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments

N.º K: K151036 · 2016-02-01

Fecha de decisión2016-02-01

Código de productoGCJ

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments 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 2016-02-01 under 510(k) number K151036. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments?

Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments is a medical device that received FDA 510(k) clearance on 2016-02-01. The listed applicant is Carefusion 2200, Inc.. The 510(k) number is K151036.

When did Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments receive FDA 510(k) clearance?

Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments received FDA 510(k) clearance on 2016-02-01, under 510(k) number K151036.

Who is the listed applicant for Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments?

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 Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments?

The FDA product code for Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic Instruments is GCJ.

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 K162432Multi-Link X2 ECG Cable and Lead Wire System K160764AirLife Autofill Humidification Chamber K153554Genesis Low Temperature Reusable Rigid Container System

Dispositivos relacionados (Código: GCJ)

K262397CuratOR EX2742Eizo Corporation K260884UNIDRIVE Select SystemKarl Storz SE & CO. KG K260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony Corporation K261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLC K253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical Impact K261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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.