FDA 510(k)

EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter

N.º K: K210313 · 2022-12-30

SolicitanteShanghai Microport EP Medtech Co., Ltd.

Fecha de decisión2022-12-30

Código de productoDRF

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Microport EP Medtech Co., Ltd.. It received FDA 510(k) clearance on 2022-12-30 under 510(k) number K210313. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter?

EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter is a medical device that received FDA 510(k) clearance on 2022-12-30. The listed applicant is Shanghai Microport EP Medtech Co., Ltd.. The 510(k) number is K210313.

When did EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter receive FDA 510(k) clearance?

EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter received FDA 510(k) clearance on 2022-12-30, under 510(k) number K210313.

Who is the listed applicant for EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter?

The FDA 510(k) record lists Shanghai Microport EP Medtech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter?

The FDA product code for EasyFinder Fixed Curve Diagnostic Catheter, Forlnk Cable for Mapping Catheter is DRF.

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 Shanghai Microport EP Medtech Co., Ltd. como solicitante

K212625PathBuilder Transseptal Needle K212626PathBuilder Transseptal Guiding Introducer K211530PathBuilder Steerable Introducer

Dispositivos relacionados (Código: DRF)

K252794Vision-MR™ Diagnostic CatheterImricor Medical Systems, Inc.K250590MAGiC Sweep™ EP Mapping CatheterStereotaxis, Inc.K250310VIKING™ Fixed Curve Diagnostic CatheterBoston Scientific Corporation K240366EP•XT™ Unidirectional Steerable Diagnostic Catheter; Dynamic Tip™ Unidirectional Steerable Diagnostic Catheter; Dynamic XT™ Unidirectional Steerable Diagnostic CatheterBoston Scientific Corporation K233900Nordica PV Cryo Mapping CatheterSynaptic Medical Corporation K233397Cosine-10TM Diagnostic CatheterMedtronic, 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.