FDA 510(k)

CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC

N.º K: K153423 · 2016-01-28

SolicitanteArrow International, Inc. (Subsidiary of Teleflex, Inc.)

Fecha de decisión2016-01-28

Código de productoLJS

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC is the device name listed in this FDA 510(k) record. The listed applicant is Arrow International, Inc. (Subsidiary of Teleflex, Inc.). It received FDA 510(k) clearance on 2016-01-28 under 510(k) number K153423. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC?

CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC is a medical device that received FDA 510(k) clearance on 2016-01-28. The listed applicant is Arrow International, Inc. (Subsidiary of Teleflex, Inc.). The 510(k) number is K153423.

When did CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC receive FDA 510(k) clearance?

CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC received FDA 510(k) clearance on 2016-01-28, under 510(k) number K153423.

Who is the listed applicant for CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC?

The FDA 510(k) record lists Arrow International, Inc. (Subsidiary of Teleflex, Inc.) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC?

The FDA product code for CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC is LJS.

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 Arrow International, Inc. (Subsidiary of Teleflex, Inc.) como solicitante

K180395EZ-IO Intraosseous Vascular Access System K163513Sistema de catéter periférico de residencia prolongada Arrow Endurance K161313ARROW Catéter Inyectable de Línea Media con Tecnología Antimicrobiana y Antitrombógena Chlorag+ard K160018Dispositivo de Cateterización Arterial Quickflash Arrow K153487CG+ Arrow PICC powered by Arrow VPS Stylet PLUS and Arrow VPS Stylet PLUS

Dispositivos relacionados (Código: LJS)

K260929Neonav ECG Tip Location SystemNavi Medical Technologies K252373BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve TechnologySpectrum Vascular K252792PM2™ System with ECGuide™ ConnectorPiccolo Medical, Inc.K243458HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit (70002302); HydroPICC 5Fr Dual Lumen Marked catheter - Maximal Barrier kit (70002304); HydrAccess Vascular, Inc.K251212Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC Catheter (PICC-252CM) (PICC-252CM)Access Vascular, Inc.K243484PM2+ System and SmartPICC StyletPiccolo Medical, 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.