Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

FDA 510(k)

Micropuncture Introducer Sets; Micropuncture Pedal Access Sets

N.º K: K240589 · 2024-03-25

SolicitanteCook Medical
Fecha de decisión2024-03-25
Código de productoDYB
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

Micropuncture Introducer Sets; Micropuncture Pedal Access Sets is the device name listed in this FDA 510(k) record. The listed applicant is Cook Medical. It received FDA 510(k) clearance on 2024-03-25 under 510(k) number K240589. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Micropuncture Introducer Sets; Micropuncture Pedal Access Sets?

Micropuncture Introducer Sets; Micropuncture Pedal Access Sets is a medical device that received FDA 510(k) clearance on 2024-03-25. The listed applicant is Cook Medical. The 510(k) number is K240589.

When did Micropuncture Introducer Sets; Micropuncture Pedal Access Sets receive FDA 510(k) clearance?

Micropuncture Introducer Sets; Micropuncture Pedal Access Sets received FDA 510(k) clearance on 2024-03-25, under 510(k) number K240589.

Who is the listed applicant for Micropuncture Introducer Sets; Micropuncture Pedal Access Sets?

The FDA 510(k) record lists Cook Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Micropuncture Introducer Sets; Micropuncture Pedal Access Sets?

The FDA product code for Micropuncture Introducer Sets; Micropuncture Pedal Access Sets is DYB.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Dispositivos relacionados (Código: DYB)

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.

K253526NAMIC Dilator and SheathMedline Industries, LPK261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line Tearaway IntroducerHealth Line International CorporationK261492FieldFlex Steerable SheathCenterPoint Systems, LLCK260606Echo Large Bore Introducer SheathEcho Medical, LLC

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.

↑