FDA 510(k)

CROSSER CTO Recanalization Catheter

N.º K: K161208 · 2016-05-24

SolicitanteBard Peripheral Vacular, Inc.

Fecha de decisión2016-05-24

Código de productoPDU

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

CROSSER CTO Recanalization Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vacular, Inc.. It received FDA 510(k) clearance on 2016-05-24 under 510(k) number K161208. The device is classified under product code PDU. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CROSSER CTO Recanalization Catheter?

CROSSER CTO Recanalization Catheter is a medical device that received FDA 510(k) clearance on 2016-05-24. The listed applicant is Bard Peripheral Vacular, Inc.. The 510(k) number is K161208.

When did CROSSER CTO Recanalization Catheter receive FDA 510(k) clearance?

CROSSER CTO Recanalization Catheter received FDA 510(k) clearance on 2016-05-24, under 510(k) number K161208.

Who is the listed applicant for CROSSER CTO Recanalization Catheter?

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

What is the FDA product code for CROSSER CTO Recanalization Catheter?

The FDA product code for CROSSER CTO Recanalization Catheter is PDU.

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: PDU)

K262013Kiba CTO Crossing CatheterReflow Medical, Inc.K252315Santreva™-ATK Endovascular Revasculariztion CatheterAngioSafe, Inc.K251158PowerWire® 14 Radiofrequency Guidewire KitBaylis Medical Technologies, Inc.K251376LimFlow ARCLimFlow, Inc.K232562PowerWire Radiofrequency Guidewire KitBaylis Medical Technologies, Inc.K230159SoundBite® Crossing System XS PeripheralSoundbite Medical Solutions, 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.