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FDA 510(k)

CardioCurve Steerable Sheath

N.º K: K210185 · 2021-07-23

SolicitanteTalon Surgical
Fecha de decisión2021-07-23
Código de productoDYB
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

CardioCurve Steerable Sheath is the device name listed in this FDA 510(k) record. The listed applicant is Talon Surgical. It received FDA 510(k) clearance on 2021-07-23 under 510(k) number K210185. 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 CardioCurve Steerable Sheath?

CardioCurve Steerable Sheath is a medical device that received FDA 510(k) clearance on 2021-07-23. The listed applicant is Talon Surgical. The 510(k) number is K210185.

When did CardioCurve Steerable Sheath receive FDA 510(k) clearance?

CardioCurve Steerable Sheath received FDA 510(k) clearance on 2021-07-23, under 510(k) number K210185.

Who is the listed applicant for CardioCurve Steerable Sheath?

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

What is the FDA product code for CardioCurve Steerable Sheath?

The FDA product code for CardioCurve Steerable Sheath is DYB.

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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.

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